279900
(S)-(+)-2-苯基丙酸
97%
别名:
(S)-(+)-氢化阿托酸, (S)-HTA
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关于此项目
线性分子式:
CH3CH(C6H5)CO2H
化学文摘社编号:
分子量:
150.17
UNSPSC Code:
12352002
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2044507
Assay:
97%
Form:
solid
InChI
1S/C9H10O2/c1-7(9(10)11)8-5-3-2-4-6-8/h2-7H,1H3,(H,10,11)/t7-/m0/s1
SMILES string
C[C@H](C(O)=O)c1ccccc1
InChI key
YPGCWEMNNLXISK-ZETCQYMHSA-N
assay
97%
form
solid
optical activity
[α]20/D +72°, c = 1.6 in chloroform
optical purity
ee: 98% (HPLC)
refractive index
n20/D 1.522 (lit.)
bp
115 °C/1 mmHg (lit.)
mp
29-30 °C (lit.)
density
1.1 g/mL at 25 °C (lit.)
functional group
carboxylic acid, phenyl
Quality Level
Application
手性结构单元。拆分剂
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
>235.4 °F - closed cup
flash_point_c
> 113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
D Ahmad et al.
Chirality, 6(5), 365-371 (1994-01-01)
The significance of disturbances of lipid metabolism caused by xenobiotic acyl-CoAs as possible causes of peroxisomal proliferation has been studied with the enantiomers of 2-phenylpropionic acid (2-PPA), the (R)-enantiomer of which is converted to the acyl-CoA in rats while its
M J Thomason et al.
Chirality, 9(3), 254-260 (1997-01-01)
Previous investigations have described the development of nongrowing suspensions of Verticillium lecanii as a microbial model of the mammalian chiral inversion of the 2-arylpropionic acids (2-APAs). Mechanistic studies in mammals have shown that inversion involves loss of the alpha-methine proton
M Sajewicz et al.
Journal of chromatographic science, 43(10), 542-548 (2006-01-28)
The usefulness of thin-layer chromatography (TLC) as an efficient measuring technique in the studies of oscillatory trans-enantiomerization of profens from the S to the R configuration (and vice versa) during their storage as 70% ethanol solutions is demonstrated in the
Chunze Li et al.
Chemical research in toxicology, 15(10), 1309-1317 (2002-10-22)
Chemically reactive species formed from the metabolism of carboxylic acid-containing compounds have been proposed as mediators of their toxic side-effects. Two alternative metabolic pathways known to be involved in the generation of reactive acylating metabolites of carboxylic acids are acyl
T Yamaguchi et al.
Drug metabolism and disposition: the biological fate of chemicals, 15(4), 535-539 (1987-07-01)
The contribution of the liver and kidney to the optical isomerization of (R)-(-)-2-phenylpropionic acid (hydratropic acid (HTA] was examined by iv injection of racemic HTA (20 mg/kg) to nephrectomized and bile duct-ligated rats (NEBL-rats), eviscerated rats with nonfunctioning livers (EVIS-rats)
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