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异丁酰氯

一般危化品
异丁酰氯结构式
异丁酰氯结构式
常用名 异丁酰氯 英文名 2-Methylpropanoyl chloride
CAS号 79-30-1 分子量 106.551
密度 1.0±0.1 g/cm3 沸点 90.9±8.0 °C at 760 mmHg
分子式 C4H7ClO 熔点 -90 °C
MSDS 中文版 美版 闪点 1.1±0.0 °C
符号 GHS02 GHS05
GHS02, GHS05
信号词 Danger

Fumigant toxicity and acetylcholinesterase inhibitory activity of 4 Asteraceae plant essential oils and their constituents against Japanese termite (Reticulitermes speratus Kolbe).

Pestic. Biochem. Physiol. 113 , 55-61, (2014)

This study investigated the fumigant toxicity of 4 Asteraceae plant essential oils and their constituents against the Japanese termite Reticulitermes speratus Kolbe. Fumigant toxicity varied with plant essential oils or constituents, exposure time, and concen...

Chimeric RNA Oligonucleotides with Triazole and Phosphate Linkages: Synthesis and RNA Interference.

Chem. Asian J. 10 , 2683-8, (2016)

Chimeric RNA oligonucleotides with an artificial triazole linker were synthesized using solution-phase click chemistry and solid-phase automated synthesis. Scalable synthesis methods for jointing units for the chimeric structure have been developed, and after...

Identification of shikonin and its ester derivatives from the roots ofEchium italicumL.

J. Chromatogr. A. 1216(15) , 3156-3162, (2009)

Nine shikonin pigments: shikonin (S), acetylshikonin (AS), propionylshikonin (PS), isobutyrylshikonin (IBS), tiglylshikonin (TS), 3,3-dimethylacrylshikonin (DAS), angelylshikonin (ANS), 2-methyl- n-butyrylshikonin (MBS) and isovalerylshikonin (IVS) were ident...

Observation of two N2-isobutyrylguanine tautomers by NMR spectroscopy.

Magn. Reson. Chem. 51(1) , 60-4, (2013)

N(2)-isobutyrylguanine was prepared by treatment of guanine with isobutyryl chloride. Two tautomers, 1,7-dihydro-2-(isobutyroyl)amino-6H-purin-6-one and 1,9-dihydro-2-(isobutyroyl)amino-6H-purin-6-one, were identified in almost 1:1 ratio in dichloromethane-di...

Tetrahedron Lett. 34 , 211, (1993)

Bioorg. Med. Chem. Lett. 3 , 1207, (1993)

Heteroatom Chem. 4 , 39, (1993)

Thermoresponsive hyperbranched polyethylenimines with isobutyramide functional groups. Liu H, et al.

J. Polym. Sci. A Polym. Chem. 45(6) , 1177-1184, (2007)