A71352
对氨基苯乙酸
98%
别名:
2-(4-Aminophenyl)acetic acid, 4-Aminobenzeneacetic acid
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关于此项目
线性分子式:
H2NC6H4CH2CO2H
化学文摘社编号:
分子量:
151.16
UNSPSC Code:
12352106
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-828-7
Beilstein/REAXYS Number:
2208094
MDL number:
Quality Level
assay
98%
form
powder
reaction suitability
reaction type: solution phase peptide synthesis
color
light yellow to tan
mp
201 °C (dec.) (lit.)
application(s)
peptide synthesis
SMILES string
Nc1ccc(CC(O)=O)cc1
InChI
1S/C8H9NO2/c9-7-3-1-6(2-4-7)5-8(10)11/h1-4H,5,9H2,(H,10,11)
InChI key
CSEWAUGPAQPMDC-UHFFFAOYSA-N
flash_point_f
Not applicable
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
D Meredith et al.
The Journal of physiology, 512 ( Pt 3), 629-634 (1999-01-09)
1. 4-Aminomethylbenzoic acid, a molecule which mimics the special configuration of a dipeptide, competitively inhibits peptide influx in both Xenopus Laevis oocytes expressing rabbit PepT1 and through PepT1 in rat renal brush border membrane vesicles. 2. This molecule is not
Douglas C McVey et al.
Digestive diseases and sciences, 50(3), 565-573 (2005-04-07)
A new compound, APAZA, consisting of a molecule of 5-aminosalicylic acid linked to one molecule of 4-aminophenylacetic acid by an azo bond, was testedfor its ability to inhibit acute colitis in rats caused by Clostridium difficile toxin A. When administered
Ahmed H Bedair et al.
Acta pharmaceutica (Zagreb, Croatia), 56(3), 273-284 (2006-09-01)
Condensation of 4-aminophenylacetic acid with phthalic anhydride gave (dioxoisoindolin-2-yl)phenylacetic acid (1), which was employed as the key intermediate in the synthesis of title compounds 2-8. The products were characterized by analytical and spectral data (IR, 1H NMR, 13C NMR and
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| A71352-100G | 04061838352309 |
| A71352-25G | 04061833383674 |