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Merck
CN

127671

3-氨基苯甲酸

98%, for peptide synthesis

别名:

3-Aminobenzenecarboxylic acid, 3-Carboxyaniline, m-Aminobenzoic acid, Aniline-3-carboxylic acid

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关于此项目

线性分子式:
H2NC6H4CO2H
化学文摘社编号:
分子量:
137.14
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352106
EC Number:
202-724-4
MDL number:
Beilstein/REAXYS Number:
471603
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产品名称

3-氨基苯甲酸, 98%

Quality Level

assay

98%

reaction suitability

reaction type: solution phase peptide synthesis

mp

178-180 °C (lit.)

application(s)

peptide synthesis

SMILES string

Nc1cccc(c1)C(O)=O

InChI

1S/C7H7NO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,8H2,(H,9,10)

InChI key

XFDUHJPVQKIXHO-UHFFFAOYSA-N



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存储类别

11 - Combustible Solids

wgk

WGK 2

flash_point_f

302.0 °F - closed cup

flash_point_c

150 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Lari Lehtiö et al.
Journal of medicinal chemistry, 52(9), 3108-3111 (2009-04-10)
Poly(ADP-ribose) polymerases (PARPs) activate DNA repair mechanisms upon stress- and cytotoxin-induced DNA damage, and inhibition of PARP activity is a lead in cancer drug therapy. We present a structural and functional analysis of the PARP domain of human PARP-3 in
Mark Eisenberg et al.
Science (New York, N.Y.), 301(5636), 1102-1104 (2003-08-23)
In memory consolidation, the memory trace stabilizes and becomes resistant to certain amnesic agents. The textbook account is that for any memorized item, consolidation starts and ends just once. However, evidence has accumulated that upon activation in retrieval, the trace
K Kakehi et al.
Journal of chromatography. A, 863(2), 205-218 (1999-12-11)
The efficiencies in derivatization of reducing carbohydrates were compared by capillary electrophoresis using maltose as a model with nine monoaminobenzene derivatives by reductive amination in the presence of sodium cyanoborohydride. We found that aminobenzene derivatives substituted at the 3-position showed



全球贸易项目编号

货号GTIN
127671-100G04061838725028
127671-25G04061838725035
127671-500G04061838725042