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Merck
CN

691445

4-氨基-3-氯苯甲酸

97%

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关于此项目

经验公式(希尔记法):
C7H6ClNO2
化学文摘社编号:
分子量:
171.58
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352106
EC Number:
219-630-4
MDL number:
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assay

97%

form

solid

reaction suitability

reaction type: solution phase peptide synthesis

mp

224-229 °C

application(s)

peptide synthesis

SMILES string

Nc1ccc(cc1Cl)C(O)=O

InChI

1S/C7H6ClNO2/c8-5-3-4(7(10)11)1-2-6(5)9/h1-3H,9H2,(H,10,11)

InChI key

YIYBPEDZAUFQLO-UHFFFAOYSA-N



pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

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

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历史批次信息供参考:

分析证书(COA)

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Z W She et al.
Free radical biology & medicine, 22(6), 989-998 (1997-01-01)
This study was designed to develop traps for hypochlorous acid (HOCl) which could be used to detect HOCl in the microenvironment of activated neutrophils. Reagent HOCl was found to react with para-aminobenzoic acid (PABA) in aqueous solution to produce a
Tomasz Frączek et al.
Journal of enzyme inhibition and medicinal chemistry, 31(3), 481-489 (2015-05-06)
Azoles are a promising class of the new generation of HIV-1 non-nucleoside reverse transcriptase inhibitors (NNRTIs). From thousands of reported compounds, many possess the same basic structure of an aryl substituted azole ring linked by a thioglycolamide chain with another



全球贸易项目编号

货号GTIN
691445-1G04061826104002
691445-5G04061832765648