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Merck
CN

538396

Sigma-Aldrich

3,4-二羟基苯腈

97%

别名:

3,4-二羟基苯甲腈

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About This Item

线性分子式:
(OH)2C6H3CN
CAS号:
分子量:
135.12
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

方案

97%

mp

155-159 °C (lit.)

官能团

nitrile

SMILES字符串

Oc1ccc(cc1O)C#N

InChI

1S/C7H5NO2/c8-4-5-1-2-6(9)7(10)3-5/h1-3,9-10H

InChI key

NUWHYWYSMAPBHK-UHFFFAOYSA-N

一般描述

3,4-二羟基苄腈可由4-羟基-3-甲氧基苄腈制备。 它也可以通过3,4-二甲氧基苄腈、二异丙基氨基锂(LDA)和1,3-二甲基-2-咪唑烷酮(DMEU)的反应来合成。

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Sodium Bis (trimethylsilyl) amide and Lithium Diisopropylamide in Deprotection of Alkyl Aryl Ethers: a-Effect of Silicon
Hwu JR, et al.
The Journal of Organic Chemistry, 62.12 , 4097-4104 (1997)
The synthetic technology of 3, 4-dihydroxybenzonitrile
WEI HW, et al.
Fine and Specialty Chemicals / Jing Xi Yu Zhuan Yong Hua Xue Pin, 9, 012-012 (2011)
M M Wick et al.
Journal of pharmaceutical sciences, 76(7), 513-515 (1987-07-01)
This report describes a structure-activity analysis of isomers of three classes of dihydroxybenzene derivatives, including dihydroxybenzaldoxime, dihydroxybenzaldehyde, and dihydroxybenzonitrile. These derivatives were examined for their effect on ribonucleotide reductase activity, macromolecular synthesis, cell growth, and in vivo antitumor activity against
M J Nelson et al.
Biochemistry, 34(46), 15219-15229 (1995-11-21)
Ferric soybean lipoxygenase forms stable complexes with 4-substituted catechols. The structure of the complex between the enzyme and 3,4-dihydroxybenzonitrile has been studied by resonance Raman, electron paramagnetic resonance, visible, and X-ray spectroscopies. It is a bidentate iron-catecholate complex with at
Pablo Salgado et al.
Environmental science & technology, 51(7), 3687-3693 (2017-03-09)
Fenton systems are interesting alternatives to advanced oxidation processes (AOPs) applied in soil or water remediation. 1,2-Dihydroxybenzenes (1,2-DHBs) are able to amplify the reactivity of Fenton systems and have been extensively studied in biological systems and for AOP applications. To

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