213853
α-乙酰氨基肉桂酸
98%
别名:
N-乙酰基脱氢苯丙氨酸
登录 查看组织和合同定价。
选择尺寸
变更视图
关于此项目
线性分子式:
C6H5CH=C(NHCOCH3)COOH
化学文摘社编号:
分子量:
205.21
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
226-795-6
Beilstein/REAXYS Number:
1912549
MDL number:
Assay:
98%
assay
98%
mp
188-190 °C (lit.)
solubility
methanol: soluble 100 mg/mL, clear, yellow-green, 95% ethanol: soluble 5%, clear, yellow
SMILES string
CC(=O)N\C(=C/c1ccccc1)C(O)=O
InChI
1S/C11H11NO3/c1-8(13)12-10(11(14)15)7-9-5-3-2-4-6-9/h2-7H,1H3,(H,12,13)(H,14,15)/b10-7-
InChI key
XODAOBAZOQSFDS-YFHOEESVSA-N
General description
Asymmeteric hydrogenation of α-acetamidocinnamic acid with chiral rhodium (I) complexes on charcoal has been reported. α-Acetamidocinnamic acid undergoes asymmetric hydrogenation in ionic liquid catalyzed by rhodium complex to yield (S)-phenylalanine.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Choong Eui Song
Chemical communications (Cambridge, England), 9(9), 1033-1043 (2004-04-30)
Recent developments in the enantioselective chemo- and bio-catalysis in ionic liquids are reviewed. In many cases, the use of ionic liquids provides many advantages over reactions in conventional organic solvents in terms of activity, enantioselectivity, stability and the reusability of
Asymmetric hydrogenation of a-acetamidocinnamic acid with chiral rhodium complexes of DIOP and BPPM on charcoal.
Masami I, et al.
Chemical & Pharmaceutical Bulletin, 31(10), 3371-3376 (1983)
全球贸易项目编号
| 货号 | GTIN |
|---|---|
| 213853-25G | 04061831819106 |
我们的科学家团队拥有各种研究领域经验，包括生命科学、材料科学、化学合成、色谱、分析及许多其他领域.
联系客户支持