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52794-98-6

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52794-98-6 Usage

Uses

3,4-Dichloro-D-phenylalanine is used in the synthesis of human Pin1 inhibitors. It is also used to prepare morphiceptin analogs with μ-receptor binding activities in brain and mammary adenocarcinoma.

Check Digit Verification of cas no

The CAS Registry Mumber 52794-98-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,7,9 and 4 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 52794-98:
(7*5)+(6*2)+(5*7)+(4*9)+(3*4)+(2*9)+(1*8)=156
156 % 10 = 6
So 52794-98-6 is a valid CAS Registry Number.
InChI:InChI=1/C9H9Cl2NO2/c10-6-2-1-5(3-7(6)11)4-8(12)9(13)14/h1-3,8H,4,12H2,(H,13,14)/t8-/m1/s1

52794-98-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (R)-2-Amino-3-(3,4-dichlorophenyl)propanoic acid

1.2 Other means of identification

Product number -
Other names D-3,4-Dichloro Phenylalanine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:52794-98-6 SDS

52794-98-6Relevant articles and documents

Enantioselective scavenging using homogenate of Rhodotorula graminis: a facile preparation of d-amino acid derivatives in enantiopure form

Zhang, Zizhang

body text, p. 6468 - 6470 (2009/04/06)

An enantioselective scavenger (ES) comprised homogenate of Rhodotorula graminis containing multiple enzymes can enantioselectively remove l-enantiomer in a racemic mixture of amino acid derivatives (AADs), yielding d-enantiomer in high ee. Thirteen non-proteinogenic AADs were produced in enantiopure d form. The method appears to be an efficient cleaning and preparative strategy which can be applied to the production of d-AADs in high ee by enantioselectively scavenging the 'l-contaminants'.

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