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S-(carboxymethyl)homocysteine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

55593-14-1

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55593-14-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 55593-14-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,5,5,9 and 3 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 55593-14:
(7*5)+(6*5)+(5*5)+(4*9)+(3*3)+(2*1)+(1*4)=141
141 % 10 = 1
So 55593-14-1 is a valid CAS Registry Number.

55593-14-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-amino-4-(carboxymethylsulfanyl)butanoic acid

1.2 Other means of identification

Product number -
Other names S-Carboxymethyl-homocystein

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:55593-14-1 SDS

55593-14-1Downstream Products

55593-14-1Relevant academic research and scientific papers

Rationally engineered variants of S-adenosylmethionine (SAM) synthase: Reduced product inhibition and synthesis of artificial cofactor homologues

Dippe,Brandt,Rost,Porzel,Schmidt,Wessjohann

supporting information, p. 3637 - 3640 (2015/03/30)

S-Adenosylmethionine (SAM) synthase was engineered for biocatalytic production of SAM and long-chain analogues by rational re-design. Substitution of two conserved isoleucine residues extended the substrate spectrum of the enzyme to artificial S-alkylhomocysteines. The variants proved to be beneficial in preparative synthesis of SAM (and analogues) due to a much reduced product inhibition. This journal is

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