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)
Hongye Zhang et al.
Journal of colloid and interface science, 338(2), 468-473 (2009-07-21)
Monodispersed TiO2 hybrid microspheres were prepared via the hydrolysis of titanium isopropoxide (TTIP) in ethanol solution containing p-aminophenylacetic acid (APA). The effects of the APA:TTIP molar ratio, water content, reaction time and reaction temperature on the morphology of the resultant
C S Temple et al.
The Journal of biological chemistry, 273(1), 20-22 (1998-02-07)
4-Aminophenylacetic acid (4-APAA), a peptide mimic lacking a peptide bond, has been shown to interact with a proton-coupled oligopeptide transporter using a number of different experimental approaches. In addition to inhibiting transport of labeled peptides, these studies show that 4-APAA
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 |