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Merck
CN

236454

Sigma-Aldrich

邻氨基苯甲酸甲酯

ReagentPlus®, ≥99%

别名:

邻氨基苯甲酸甲酯

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关于此项目

线性分子式:
2-(H2N)C6H4CO2CH3
化学文摘社编号:
分子量:
151.16
Beilstein:
606965
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽压

1 mmHg ( 20 °C)

产品线

ReagentPlus®

方案

≥99%

表单

liquid

自燃温度

986 °F

折射率

n20/D 1.582 (lit.)

沸点

256 °C (lit.)

mp

24 °C (lit.)

溶解性

alcohol: freely soluble(lit.)
diethyl ether: freely soluble(lit.)
water: slightly soluble(lit.)

密度

1.168 g/mL at 25 °C (lit.)

官能团

ester

SMILES字符串

COC(=O)c1ccccc1N

InChI

1S/C8H9NO2/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5H,9H2,1H3

InChI key

VAMXMNNIEUEQDV-UHFFFAOYSA-N

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一般描述

2-氨基苯甲酸甲酯在140°C下可与2,4-(4-甲氧基苯基)-1,3,2,4-二硫代二膦-2,4-二硫化物反应生成1,2-二氢-2-(甲氧基苯基)-4H-3,1,2-苯并噻唑磷酰-4-硫酮-2-硫化物和4-甲氧基苯基三硫代磷酸二甲酯

应用

2-氨基苯甲酸甲酯已被用于合成新型4-氯-2-巯基苯磺酰胺衍生物

法律信息

ReagentPlus is a registered trademark of Merck KGaA, Darmstadt, Germany

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2

储存分类代码

10 - Combustible liquids

WGK

WGK 1

闪点(°F)

262.4 °F - closed cup

闪点(°C)

128 °C - closed cup

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Studies on organophosphorus compounds-XXXVI: simple new routes to phosphorins from 2-hydroxy-, 2-mercapto-, and 2-aminobenzoic acids and their derivatives.
El-Barbary AA and Lawesson S-O.
Tetrahedron, 37(15), 2641-2646 (1981)
I M Li de La Sierra et al.
Biochemistry, 39(51), 15870-15878 (2000-12-22)
The conformation and dynamics of the ATP binding site of cytidine monophosphate kinase from Escherichia coli (CMPK(coli)), which catalyzes specifically the phosphate exchange between ATP and CMP, was studied using the fluorescence properties of 3'-anthraniloyl-2'-deoxy-ADP, a specific ligand of the
Marie E Gibbs et al.
Brain research bulletin, 76(3), 198-207 (2008-05-24)
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The biosynthesis of methyl anthranilate, the volatile compound responsible for the distinctive 'foxy' aroma and flavor of the Washington Concord grape (Vitis labrusca), involves an alcohol acyltransferase that catalyzes the formation of methyl anthranilate from anthraniloyl-coenzyme A (CoA) and methanol.
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