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Merck
CN

419443

Sigma-Aldrich

2-氨基-5-甲基苯甲酸

99%

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别名:
5-甲基邻氨基苯甲酸
线性分子式:
H2NC6H3(CH3)CO2H
CAS号:
分子量:
151.16
Beilstein:
1101527
EC 号:
MDL编号:
UNSPSC代码:
12352106
eCl@ss:
32160406
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

99%

反应适用性

reaction type: solution phase peptide synthesis

mp

175 °C (dec.) (lit.)

应用

peptide synthesis

SMILES字符串

Cc1ccc(N)c(c1)C(O)=O

InChI

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

InChI key

NBUUUJWWOARGNW-UHFFFAOYSA-N

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一般描述

2-Amino-5-methylbenzoic acid also known as 5-methylanthranilic acid, is often used in the solution-phase peptide synthesis.

应用

2-Amino-5-methylbenzoic acid can be used to synthesize quinazolinedione.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

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


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Synthesis and evaluation of quinazolines as inhibitors of the bacterial cell division protein FtsZ
GM Nepomuceno
ACS Medicinal Chemistry Letters, 6, 308-312 (2015)
João Daniel Santos Fernandes et al.
PloS one, 10(7), e0132369-e0132369 (2015-07-15)
Metabolic diversity is an important factor during microbial adaptation to different environments. Among metabolic processes, amino acid biosynthesis has been demonstrated to be relevant for survival for many microbial pathogens, whereas the association between pathogenesis and amino acid uptake and

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