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120881-97-2

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120881-97-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 120881-97-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,0,8,8 and 1 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 120881-97:
(8*1)+(7*2)+(6*0)+(5*8)+(4*8)+(3*1)+(2*9)+(1*7)=122
122 % 10 = 2
So 120881-97-2 is a valid CAS Registry Number.

120881-97-2SDS

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)-1-Methyl-2-oxo-but-3-enyl)-carbamic acid tert-butyl ester

1.2 Other means of identification

Product number -
Other names -

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:120881-97-2 SDS

120881-97-2Downstream Products

120881-97-2Relevant articles and documents

(3-Amino-2-oxoalkyl)phosphnic Acids and Their Analogues as Novel Inhibitors of D-Alanine: D-alanine Ligase

Chakravarty, Prasun K.,Greenlee, William J.,Parsons, William H.,Patchett, Arthur A.,Combs, Patricia,et al.

, p. 1886 - 1890 (1989)

The dipeptide D-alanyl-D-alanine is an essential precursor of bacterial peptidoglycan; thus, blocking its formation is a possible target for the design of novel antibacterial agents.The synthesis of this dipeptide by bacterial D-alanine:D-alanine ligase requires ATP.In analogy with glutamine synthetase, we hypothesized a mechanism for this enzyme involving the intermediacy of D-alanyl phosphate.Several (3-amino-2-oxoalkyl)phosphonic acids and their analogues have been synthesized as possible inhibitory mimics of this proposed intermediate.The most active of them, (3(R)-amino-2-oxobutyl)phosphonic acid (8a) and the corresponding aza analogue (22), were effective ligase inhibitors although they had no significant antibacterial activity.The ligase inhibition of these compounds is consistent with an acyl phosphate displacement step in the mechanism of DAla-DAla ligase.

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