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Merck
CN

258040

Sigma-Aldrich

3,4-二甲氧基苯甲酰氯

98%

别名:

藜芦酰氯

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About This Item

线性分子式:
(CH3O)2C6H3COCl
CAS号:
分子量:
200.62
Beilstein:
783596
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

98%

表单

solid

mp

70-73 °C (lit.)

官能团

acyl chloride

SMILES字符串

COc1ccc(cc1OC)C(Cl)=O

InChI

1S/C9H9ClO3/c1-12-7-4-3-6(9(10)11)5-8(7)13-2/h3-5H,1-2H3

InChI key

VIOBGCWEHLRBEP-UHFFFAOYSA-N

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应用

3,4-Dimethoxybenzoyl chloride has been used in synthesis of:
  • (+)-5-(3,4-dimethoxyphenyl)-4-[[N-[(4S)-2-oxo-4-(phenylmethyl)-2-oxazolidinyl]]carbonyl] oxazole and its enantiomer
  • N-(2,5-dibromophenyl)-3,4-dimethoxybenzamide

象形图

Corrosion

警示用语:

Danger

危险声明

危险分类

Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Jian S. Tang et al.
The Journal of organic chemistry, 61(25), 8750-8754 (1996-12-13)
Both (4S-(+)-3-(isocyanoacetyl)-4-(phenylmethyl)-2-oxazolidinone (R)-1 and its enantiomer (S)-1 have been synthesized as potentially useful synthons in asymmetric synthesis. Optically active (+)-5-(3,4-dimethoxyphenyl)-4-[[N-[(4S)-2-oxo-4-(phenylmethyl)-2-oxazolidinyl]]carbonyl] oxazole (S)-2 and its enantiomer (R)-2 obtained by treating 3,4-dimethoxybenzoyl chloride with (S)-1 and (R)-1, respectively, in the presence of
Catriona G Mortimer et al.
Journal of medicinal chemistry, 49(1), 179-185 (2006-01-06)
A series of new 2-phenylbenzothiazoles has been synthesized on the basis of the discovery of the potent and selective in vitro antitumor properties of 2-(3,4-dimethoxyphenyl)-5-fluorobenzothiazole (8n; GW 610, NSC 721648). Synthesis of analogues substituted in the benzothiazole ring was achieved

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