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Desamino (αS)-Chloro Histidine Methyl Ester
Cas No: 64407-67-6
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BOC Sciences
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Desamino (αS)-Chloro Histidine Methyl Ester
Cas No: 64407-67-6
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ZHEJIANG JIUZHOU CHEM CO.,LTD
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Desamino (aS)-Chloro Histidine Methyl Ester
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Finetech Industry Limited
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Desamino (αS)-Chloro Histidine Methyl Ester
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PRIME MOLECULAR CO.,LIMITED
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64407-67-6 Usage

Uses

Histidine derivative.

Check Digit Verification of cas no

The CAS Registry Mumber 64407-67-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,4,0 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 64407-67:
(7*6)+(6*4)+(5*4)+(4*0)+(3*7)+(2*6)+(1*7)=126
126 % 10 = 6
So 64407-67-6 is a valid CAS Registry Number.

64407-67-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name	methyl 3-(imidazol-4(5)-yl)-2-chloropropanoate

1.2 Other means of identification

Product number	-
Other names	Desamino (AlphaS)-Chloro Histidine Methyl Ester

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:64407-67-6 SDS

64407-67-6Upstream product

64407-67-6Downstream Products

160073-02-9 methyl 3-(imidazol-4⁽⁵⁾-yl)-2-propenoate

64407-67-6Relevant articles and documents

Efficient preparation of urocanic acid derivatives from histidine

Lovely, Carl J.,Sivappa, Rasapalli,Mukherjee, Sabuj,Doundoulakis, Thomas,Lima, Heather M.,Yousufuddin, Muhammed

, p. 1353 - 1358 (2010)

Urocanic acid derivatives have served as useful starting materials in several total synthesis endeavors in our lab. This paper describes a convenient, large-scale synthesis of several derivatives of urocanic acid via the net elimination of ammonia from hi

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CAS

64407-67-6