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关于此项目
线性分子式:
(OH)2C6H3CN
化学文摘社编号:
分子量:
135.12
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
241-367-9
MDL number:
Assay:
97%
Quality Level
assay
97%
mp
155-159 °C (lit.)
functional group
nitrile
SMILES string
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
General description
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。
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
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
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 538396-25G | 04061832566368 |