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57939-39-6

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57939-39-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 57939-39-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,3 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 57939-39:
(7*5)+(6*7)+(5*9)+(4*3)+(3*9)+(2*3)+(1*9)=176
176 % 10 = 6
So 57939-39-6 is a valid CAS Registry Number.

57939-39-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-amino-2-butylsulfanyl-1H-pyrimidin-4-one

1.2 Other means of identification

Product number -
Other names F0896-0147

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:57939-39-6 SDS

57939-39-6Relevant articles and documents

CHEMICAL COMPOUNDS - 795

-

Page/Page column 28, (2009/04/25)

The invention relates to chemical compounds, or pharmaceutically acceptable salts thereof of the formula (I): which have bacterial Murl inhibitory activity and are accordingly useful for their treatment and prophylaxis of bacterial infection, e.g., E.faec

Exploring 8-benzyl pteridine-6,7-diones as inhibitors of glutamate racemase (MurI) in Gram-positive bacteria

Breault, Gloria A.,Comita-Prevoir, Janelle,Eyermann, Charles J.,Geng, Bolin,Petrichko, Randy,Doig, Peter,Gorseth, Elise,Noonan, Brian

scheme or table, p. 6100 - 6103 (2009/07/18)

A successful scaffold-hopping approach gave a novel series of inhibitors of bacterial glutamate racemase (MurI). Early SAR studies of the 8-benzyl pteridine-6,7-diones led to compounds with micromolar enzyme potency and antibacterial activity.

Structure-based design of 2-arylamino-4-cyclohexylmethyl-5-nitroso-6-aminopyrimidine inhibitors of cyclin-dependent kinases 1 and 2

Sayle, Kerry L.,Bentley, Johanne,Boyle, F. Thomas,Calvert, A. Hilary,Cheng, Yuzhu,Curtin, Nicola J.,Endicott, Jane A.,Golding, Bernard T.,Hardcastle, Ian R.,Jewsbury, Philip,Mesguiche, Veronique,Newell, David R.,Noble, Martin E. M.,Parsons, Rachel J.,Pratt, David J.,Wang, Lan Z.,Griffin, Roger J.

, p. 3079 - 3082 (2007/10/03)

A series of O4-cyclohexylmethyl-5-nitroso-6-aminopyrimidines bearing 2-arylamino substituents was synthesised and evaluated for CDK1 and CDK2 inhibitory activity. Consistent with analogous studies with O 6-cyclohexylmethylpurines, 2-

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