溴代仲丁烷结构式
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常用名 | 溴代仲丁烷 | 英文名 | 2-Bromobutane |
|---|---|---|---|---|
| CAS号 | 78-76-2 | 分子量 | 137.018 | |
| 密度 | 1.3±0.1 g/cm3 | 沸点 | 90.7±8.0 °C at 760 mmHg | |
| 分子式 | C4H9Br | 熔点 | -112 °C | |
| MSDS | 中文版 美版 | 闪点 | 21.1±0.0 °C | |
| 符号 |
GHS02 |
信号词 | Danger |
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Validated methods for degrading hazardous chemicals: some halogenated compounds.
Am. Ind. Hyg. Assoc. J. 52(6) , 252-7, (1991) Two techniques were investigated for degrading a number of halogenated compounds of commercial and research importance. Reductive dehalogenation with nickel-aluminum alloy in potassium hydroxide solution was used to degrade iodomethane, chloroacetic acid, tri... |
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Enantioselective surface chemistry of R-2-bromobutane on Cu(643)R&S and Cu(531)R&S.
J. Phys. Chem. B 110(21) , 10411-20, (2006) The enantioselective surface chemistry of chiral R-2-bromobutane was studied on the naturally chiral Cu(643)R&S and Cu(531)R&S surfaces by comparing relative product yields during temperature-programmed reaction spectroscopy. Molecularly adsorbed R-2-bromobut... |
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Microbial growth on 2-bromobutane.
Antonie van Leeuwenhoek 46(4) , 331-41, (1980) A member of the genus Arthrobacter was isolated which grew at the expense of 2-bromobutane as sole source of carbon and energy. Evidence is presented which suggests that the initial conversion of 2-bromobutane to 2-butanol is a spontaneous chemical hydrolysis... |
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Selective Reactivity in Gas-Liqiud Chromatography. Determination of 2-Bromobutane and 1-Bromo-2-methylpropane. Harris WE and McFadden WH.
Anal. Chem. 31(1) , 114-7, (1959)
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STEREOCHEMISTRY AND ISOTOPE EFFECT IN THE DEHYDROBROMINATION OF 2-BROMOBUTANE OVER SOLID CATALYSTS. Misono M and Yoneda Y.
Chem. Lett. 1(7) , 551-2, (1972)
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Viscosities of binary mixtures of 2-bromobutane and 2-bromo-2-methylpropane with isomeric butanols at 298.15 and 313.15 K. Artigas H, et al.
Int. J. Thermophys. 23(6) , 1455-1468, (2002)
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Photobromination of (-)-(2R)-2-bromobutane with bromine-81. Tanner DD, et al.
J. Am. Chem. Soc. 99(8) , 2714-2723, (1977)
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Synthesis of non-nucleosides: 7- and 1,3-substituents of new pyrrolo[2,3-d]pyrimidin-4-ones on antiviral activity.
Arch. Pharm. (Weinheim) 339(4) , 174-81, (2006) A series of non-nucleosides 9-47 were synthesized. Compounds 1-4 were reacted with formic acid (85%) to afford compounds 5-8. Then, the latter compounds were reacted with alkyl halides a-f (2-bromopropane, 2-bromobutane, benzyl bromide, benzyl chloromethyl et... |