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Merck

691445

Sigma-Aldrich

4-氨基-3-氯苯甲酸

97%

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About This Item

经验公式(希尔记法):
C7H6ClNO2
CAS号:
分子量:
171.58
EC號碼:
MDL號碼:
分類程式碼代碼:
12352106
eCl@ss:
32160406
PubChem物質ID:

化驗

97%

形狀

solid

反應適用性

reaction type: solution phase peptide synthesis

mp

224-229 °C

應用

peptide synthesis

SMILES 字串

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 密鑰

YIYBPEDZAUFQLO-UHFFFAOYSA-N

象形圖

Exclamation mark

訊號詞

Warning

危險分類

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

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


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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
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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

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