Category: 616-14-8

So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Mori, Kenji; Yang, Chang Yeol researched the compound: 1-Iodo-2-methylbutane( cas:616-14-8 ).Related Products of 616-14-8.They published the article 《Pheromone synthesis. Part 259: Synthesis of seven methyl-branched hydrocarbons as the pheromone candidates for female Korean apricot wasp, Eurytoma maslovskii》 about this compound( cas:616-14-8 ) in Tetrahedron. Keywords: pheromone synthesis Korean apricot wasp branched hydrocarbon. We’ll tell you more about this compound (cas:616-14-8).

Seven new methyl-branched hydrocarbons were synthesized, which were the pheromone candidates of the female Korean apricot wasp (Eurytoma maslovskii). They are (Z)-15-methyl-7-nonacosene (I), (Z)-17-methyl-7-hentriacontene (II), 3,7-dimethylheptacosane (III), 8,12-dimethyltriacontane (IV), 8,18-dimethyltriacontane (V), 3,7,11-trimethylnonacosane (VI), and 3,7,17-trimethylnonacosane (VII). All of them were synthesized as stereoisomeric mixtures, employing short and simple routes. Hydrocarbon VII was synthesized via 4,8-dimethyldecanal (tribolure), the red flour beetle pheromone. The hydrocarbons I, II, III and VI were identified by GC-MS anal. as the components (with unknown stereochem.) of the female-specific secretion of E. maslovskii.

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Suzuki, Takahisa published the article 《Identification of the aggregation pheromone of flour beetles Tribolium castaneum and T. confusum (Coleoptera: Tenebrionidae)》. Keywords: pheromone aggregation Tribolium methyldecanalysis; beetle aggregation pheromone methyldecanalysis.They researched the compound: 1-Iodo-2-methylbutane( cas:616-14-8 ).Computed Properties of C5H11I. Aromatic heterocyclic compounds can be divided into two categories: single heterocyclic and fused heterocyclic. In addition, there is a lot of other information about this compound (cas:616-14-8) here.

The aggregation pheromone produced by the male red flour beetle, T. castaneum, and confused flour beetle, T. confusum, was identified as 4,8-dimethyldecan-1-al by gas-liquid chromatog., gas chromatog.-mass spectrometry, 1H NMR spectra, and synthesis of the compound The synthetic pheromone was less attractive compared with the natural pheromone, because the synthetic sample was composed of 4 optical isomers.

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Most of the compounds have physiologically active properties, and their biological properties are often attributed to the heteroatoms contained in their molecules, and most of these heteroatoms also appear in cyclic structures. A Journal, Spectrochimica Acta called The infrared spectrum of the formate ion, Author is Schutte, C. J. H.; Buijs, K., which mentions a compound: 616-14-8, SMILESS is CCC(CI)C, Molecular C5H11I, SDS of cas: 616-14-8.

The infrared spectra of anhydrous Ca(HCO2)2, Sr(HCO2)2, Ba(HCO2)2, and Pb(HCO2)2 show clearly the doubling of the fundamental bands of the formate ion owing to the existence of non-equivalent ions in the lattice. A new tetragonal phase of Ca(HCO2)2 precipitate when an organic solvent is added to an aqueous solution of Ca(HCO2)2. The new β phase belongs to space group D44-P412121, α = 9.46 A., c = 6.77 A., with 4 mols. per unit cell. The absorption bands for the β phase are single, in accordance with the crystallographic symmetry.

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Safety of 1-Iodo-2-methylbutane. So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic. Compound: 1-Iodo-2-methylbutane, is researched, Molecular C5H11I, CAS is 616-14-8, about Metal-free C(sp3)-H functionalization of sulfonamides via strain-release rearrangement.

A metal-free reaction system that enables C-H bond functionalization of aliphatic sulfonamides R(CH2)2N(F)Ts (R = decyl, cyclohexyl, oxan-4-yl, benzyl, etc.) using DABCO as a promoter under mild conditions, affording a series of α,β-unsaturated imines R1CH=C(R)CH=NTs (R1 = Ph, 4-chlorophenyl, 2,3-dihydro-1-benzofuran-5-yl, etc.) in good yields with high selectivities was presented. This protocol tolerates a broad range of functionalities and can serve as a powerful synthetic tool for the late-stage modification of complex compounds More importantly, control experiments and detailed DFT calculations suggest that this process involves [2 + 2] cyclization/ring-cleavage reorganization, which opens up a new platform for the establishment of other related reorganization reactions.

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So far, in addition to halogen atoms, other non-metallic atoms can become part of the aromatic heterocycle, and the target ring system is still aromatic.Seebach, D.; Steinmueller, D. researched the compound: 1-Iodo-2-methylbutane( cas:616-14-8 ).Application In Synthesis of 1-Iodo-2-methylbutane.They published the article 《Preparation of (S)-2-methylbutyl and (S)-sec-butyl ketones from optically active 2-methyl-1-butanol by the dithiane method》 about this compound( cas:616-14-8 ) in Angewandte Chemie, International Edition in English. Keywords: ketone; aldehyde; dithianes. We’ll tell you more about this compound (cas:616-14-8).

Optically active aldehydes and ketones EtMeCHCRO (where R = H, Me, Ph, Me3Si, C5H11, or 1-cyclohexenyl) were prepared by treating EtMeCHCHO, obtained from EtMeCHCH2OH, with CH2(CH2SH)2 to give 2-(1-methylpropyl)-1,3-dithiane, which was then alkylated and hydrolyzed. The loss of optical activity was <20% for the reaction sequence. From this literature《Preparation of (S)-2-methylbutyl and (S)-sec-butyl ketones from optically active 2-methyl-1-butanol by the dithiane method》,we know some information about this compound(616-14-8)Application In Synthesis of 1-Iodo-2-methylbutane, but this is not all information, there are many literatures related to this compound(616-14-8).

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Reference of 1-Iodo-2-methylbutane. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 1-Iodo-2-methylbutane, is researched, Molecular C5H11I, CAS is 616-14-8, about Preparation of standard mixtures of iodoalkanes by irradiation of iodine solutions in alkanes. Author is Castello, Gianrico; D’Amato, Giuseppina.

Mixtures of iodine with pentane, hexane, 3-methylpentane, 2,2-dimethylbutane, 2,3-dimethylbutane, heptane, 2,2-dimethylpentane, 2,4-dimethylpentane, 3,3-dimethylpentane, octane, 2,2,4-trimethylpentane, and 2,2,5-trimethylhexane were subjected to γ-irradiation and the gas chromatog. retention indexes of the resulting iodoalkanes determined

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Electric Literature of C5H11I. The fused heterocycle is formed by combining a benzene ring with a single heterocycle, or two or more single heterocycles. Compound: 1-Iodo-2-methylbutane, is researched, Molecular C5H11I, CAS is 616-14-8, about Pheromone synthesis. Part 259: Synthesis of seven methyl-branched hydrocarbons as the pheromone candidates for female Korean apricot wasp, Eurytoma maslovskii. Author is Mori, Kenji; Yang, Chang Yeol.

Seven new methyl-branched hydrocarbons were synthesized, which were the pheromone candidates of the female Korean apricot wasp (Eurytoma maslovskii). They are (Z)-15-methyl-7-nonacosene (I), (Z)-17-methyl-7-hentriacontene (II), 3,7-dimethylheptacosane (III), 8,12-dimethyltriacontane (IV), 8,18-dimethyltriacontane (V), 3,7,11-trimethylnonacosane (VI), and 3,7,17-trimethylnonacosane (VII). All of them were synthesized as stereoisomeric mixtures, employing short and simple routes. Hydrocarbon VII was synthesized via 4,8-dimethyldecanal (tribolure), the red flour beetle pheromone. The hydrocarbons I, II, III and VI were identified by GC-MS anal. as the components (with unknown stereochem.) of the female-specific secretion of E. maslovskii.

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In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called Total Synthesis of (-)-Cylindrocyclophane F: A Yardstick for Probing New Catalytic C-C Bond-Forming Methodologies, published in 2018, which mentions a compound: 616-14-8, Name is 1-Iodo-2-methylbutane, Molecular C5H11I, Application In Synthesis of 1-Iodo-2-methylbutane.

A short and efficient total synthesis of the C2-sym. (-)-cylindrocyclophane F is presented, using a cross olefin metathesis dimerization strategy for construction of the [7,7]-paracyclophane macrocycle. The synthesis of the dimerization building block includes a Pd-catalyzed sp3-sp2 Negishi cross coupling of a sterically hindered Zn-reagent with an aromatic triflate, an enantiospecific Zn-catalyzed sp3-sp3 cross coupling of an α-hydroxy ester triflate with a Grignard reagent and the application of an enantioselective Rh-catalyzed C-allylation of an electron rich arene.

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The reaction of an aromatic heterocycle with a proton is called a protonation. One of articles about this theory is 《Vital signs: trends in use of long-acting reversible contraception among teens aged 15-19 years seeking contraceptive services—United States, 2005-2013.》. Authors are Romero, Lisa; Pazol, Karen; Warner, Lee; Gavin, Lorrie; Moskosky, Susan; Besera, Ghenet; Loyola Briceno, Ana Carolina; Jatlaoui, Tara; Barfield, Wanda; Centers for Disease Control and Prevention (CDC).The article about the compound:1-Iodo-2-methylbutanecas:616-14-8,SMILESS:CCC(CI)C).Recommanded Product: 616-14-8. Through the article, more information about this compound (cas:616-14-8) is conveyed.

BACKGROUND: Nationally, the use of long-acting reversible contraception (LARC), specifically intrauterine devices (IUDs) and implants, by teens remains low, despite their effectiveness, safety, and ease of use. METHODS: To examine patterns in use of LARC among females aged 15-19 years seeking contraceptive services, CDC and the U.S. Department of Health and Human Services’ Office of Population Affairs analyzed 2005-2013 data from the Title X National Family Planning Program. Title X serves approximately 1 million teens each year and provides family planning and related preventive health services for low-income persons. RESULTS: Use of LARC among teens seeking contraceptive services at Title X service sites increased from 0.4% in 2005 to 7.1% in 2013 (p-value for trend <0.001). Of the 616,148 female teens seeking contraceptive services in 2013, 17,349 (2.8%) used IUDs, and 26,347 (4.3%) used implants. Use of LARC was higher among teens aged 18-19 years (7.6%) versus 15-17 years (6.5%) (p<0.001). The percentage of teens aged 15-19 years who used LARC varied widely by state, from 0.7% (Mississippi) to 25.8% (Colorado). CONCLUSIONS: Although use of LARC by teens remains low nationwide, efforts to improve access to LARC among teens seeking contraception at Title X service sites have increased use of these methods. IMPLICATIONS FOR PUBLIC HEALTH PRACTICE: Health centers that provide quality contraceptive services can facilitate use of LARC among teens seeking contraception. Strategies to address provider barriers to offering LARC include: 1) educating providers that LARC is safe for teens; 2) training providers on LARC insertion and a client-centered counseling approach that includes discussing the most effective contraceptive methods first; and 3) providing contraception at reduced or no cost to the client. From this literature《Vital signs: trends in use of long-acting reversible contraception among teens aged 15-19 years seeking contraceptive services—United States, 2005-2013.》,we know some information about this compound(616-14-8)Recommanded Product: 616-14-8, but this is not all information, there are many literatures related to this compound(616-14-8).

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In general, if the atoms that make up the ring contain heteroatoms, such rings become heterocycles, and organic compounds containing heterocycles are called heterocyclic compounds. An article called On labeling with generator nuclides, published in 1983, which mentions a compound: 616-14-8, Name is 1-Iodo-2-methylbutane, Molecular C5H11I, Application of 616-14-8.

Short-lived radioisotopes separated from radionuclide generators are widely used. The possibilities of labeling with the daughter nuclides of the com. available Mo/Tc-, Sn/In- and Te/I- generators and of the self-made Ba/La-generator in industrial tracer experiments are presented. The transfer of the daughter nuclides from the generator eluates into organic phases and the labeling of oil-phases and solid particles were investigated. The simple, quick, and efficient methods developed are suitable for routine application under industrial conditions. Some examples of industrial applications of the generator nuclides are given.

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