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66398-37-6

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66398-37-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 66398-37-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,3,9 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66398-37:
(7*6)+(6*6)+(5*3)+(4*9)+(3*8)+(2*3)+(1*7)=166
166 % 10 = 6
So 66398-37-6 is a valid CAS Registry Number.

66398-37-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S)-2-[(2-amino-3,5-dibromophenyl)methylamino]-4-methylsulfanylbutanoic acid

1.2 Other means of identification

Product number -
Other names L-Methionine,N-[(2-amino-3,5-dibromophenyl)methyl]

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:66398-37-6 SDS

66398-37-6Downstream Products

66398-37-6Relevant articles and documents

Process for the preparation of sulfur-containing N-benzyl-amino acids and esters

-

, (2008/06/13)

A process for the preparation of sulfur-containing N-benzyl-amino acids of the formula STR1 wherein X and Y, which may be identical to or different from each other, are each hydrogen or halogen; R1 is hydrogen or alkyl of 1 to 4 carbon atoms; R2 is hydrogen, alkyl of 1 to 3 carbon atoms, carboxy-lower alkyl or acyl; R3 is hydrogen or acyl; and n is 1 or 2; which comprises the steps of converting anthranilic acid or a halogenated anthranilic acid into the corresponding aldehyde, reacting the aldehyde with a compound of the formula STR2 wherein R1, R2 and n have the meanings previously defined, to form the corresponding Schiff's base, reducing the said Schiff's base, and recovering the reaction product.

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