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
产品名称
3-氨基苯甲酸, 98%
InChI key
XFDUHJPVQKIXHO-UHFFFAOYSA-N
InChI
1S/C7H7NO2/c8-6-3-1-2-5(4-6)7(9)10/h1-4H,8H2,(H,9,10)
SMILES string
Nc1cccc(c1)C(O)=O
assay
98%
reaction suitability
reaction type: solution phase peptide synthesis
mp
178-180 °C (lit.)
application(s)
peptide synthesis
Quality Level
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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
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
Julia Cuers et al.
Carbohydrate research, 348, 55-63 (2011-12-17)
Substituent patterns in oligosaccharide derivatives obtained from methyl cellulose were determined up to DP10 by electrospray ionization mass spectrometry employing separation of the oligomer fractions by HPLC. Oligosaccharides were labeled with meta-aminobenzoic acid after perdeuteromethylation and partial hydrolysis of methyl
Qiliang Deng et al.
Chemical communications (Cambridge, England), 48(24), 3009-3011 (2012-02-14)
Fluorescent conjugated polymer, poly(3-aminobenzoic acid), as a new class of fluorescence sensor for detection of trace amounts of water in organic solvents was developed. This sensor exhibits extraordinarily high sensitivity with a detection limit as low as 0.008 wt% for
Khaled H Almabruk et al.
Organic letters, 15(7), 1678-1681 (2013-03-26)
A mutasynthetic strategy has been used to generate fluorinated TM-025 and TM-026, two biosynthetically engineered pactamycin analogues produced by Streptomyces pactum ATCC 27456. The fluorinated compounds maintain excellent activity and selectivity toward chloroquine-sensitive and multidrug-resistant strains of malarial parasites as
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
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