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线性分子式:
C6H5CH(NH2)CO2H
化学文摘社编号:
分子量:
151.16
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352209
EC Number:
212-876-3
MDL number:
Beilstein/REAXYS Number:
2208676
产品名称
D-(-)-α-苯甘氨酸, 99%
Quality Level
InChI key
ZGUNAGUHMKGQNY-SSDOTTSWSA-N
InChI
1S/C8H9NO2/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5,7H,9H2,(H,10,11)/t7-/m1/s1
SMILES string
N[C@@H](C(O)=O)c1ccccc1
assay
99%
form
powder or crystals
optical activity
[α]20/D −155°, c = 1 in 1 M HCl
reaction suitability
reaction type: solution phase peptide synthesis
color
white
mp
302 °C (dec.) (lit.)
application(s)
detection
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
302.0 °F - closed cup
flash_point_c
150 °C - closed cup
ppe
Eyeshields, Gloves, type N95 (US)
Kuoxi Xu et al.
Chirality, 24(8), 646-651 (2012-05-24)
The triazine-based bisbinaphthyl crown ethers oxacalix[2]arene[2]bisbinaphthes R-1, R-2, R-3 and S-1, S-2, S-3 were synthesized. The interactions of these compounds with various α-aminocarboxylic acid anions were studied. The crown ethers were found to carry out highly enantioselective fluorescent recognition of
Martijn A Hoeben et al.
Biotechnology and bioengineering, 93(4), 607-617 (2006-01-06)
The interfacial partitioning behavior of ampicillin and phenylglycine crystals in different two-phase systems has been investigated. The two-phase systems employed are water/dodecane, water/1-butanol, and water/pentane/methanol. By means of partition experiments and microscopic imaging, it has been shown that the mechanism
Hyung Min Kim et al.
The Journal of chemical physics, 128(18), 184313-184313 (2008-06-06)
We investigated the conformational structures of L-phenylglycine in the gas phase by photoionization and double resonance spectroscopy techniques as well as high-level ab initio calculations. The UV-UV and IR-UV double resonance spectroscopy suggested that there exists only one conformer that
José Alixandre de Sousa Luis et al.
Molecules (Basel, Switzerland), 15(1), 128-137 (2010-01-30)
Hydantoins and their derivatives constitute a group of pharmaceutical compounds with anticonvulsant and antiarrhythmic properties, and are also used against diabetes. N-3 and C-5 substituted imidazolidines are examples of such products. As such, we have developed a synthesis of 2,4-dione
Shohei Tashiro et al.
Inorganic chemistry, 50(1), 4-6 (2010-12-01)
The optically active cobalt(III) complex with chiral cyclen, (2S,5S,8S,11S)-2,5,8,11-tetraethyl-1,4,7,10-tetraazacyclododecane, preferentially binds to D-phenylglycine (D-Phg) or D-t-leucine (D-t-Leu) rather than L-Phg or L-t-Leu, respectively, with 20% de in dimethyl sulfoxide at 293 K. Comparative studies on the crystal structures of cobalt(III)
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