C1503
N-Chloroacetyl-L-phenylalanine
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About This Item
Empirical Formula (Hill Notation):
C11H12ClNO3
CAS Number:
Molecular Weight:
241.67
PubChem Substance ID:
eCl@ss:
32160406
UNSPSC Code:
12352200
MDL number:
InChI
1S/C11H12ClNO3/c12-7-10(14)13-9(11(15)16)6-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,13,14)(H,15,16)/t9-/m0/s1
SMILES string
OC(=O)[C@H](Cc1ccccc1)NC(=O)CCl
InChI key
FUHGSOAURCZWCC-VIFPVBQESA-N
form
solid
technique(s)
ligand binding assay: suitable
storage temp.
−20°C
Biochem/physiol Actions
N-Chloroacetyl-L-phenylalanine is used as a substrate to identify, differentiate and characterize L-amino acid acylases such as A933 acylase. N-Chloroacetyl-L-phenylalanine may be a donor molecule in some chloroacetylation reactions.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Yi-Bing Huang et al.
Journal of biotechnology, 125(3), 311-318 (2006-04-20)
The tetrapeptide Bz-Arg-Gly-Asp-Ser-NH(2) (Bz-RGDS-NH(2)) was successfully synthesized by a combination of chemical and enzymatic methods in this study. Firstly, the precursor tripeptide Gly-Asp-Ser-NH(2) (GDS-NH(2)) was synthesized by a novel chemical method in four steps including chloroacetylation of l-aspartic acid, synthesis
K Kubo et al.
The Journal of antibiotics, 38(5), 622-630 (1985-05-01)
A933 acylase, which is involved in exchange of the pantothenyl substituent of OA-6129 carbapenems with acetyl CoA, was characterized as an L-amino acid acylase with a molecular weight of 100,000 (+/- 8,000) and a pI value of 5.1. The highest
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