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4(1H)-Pteridinone, 2-amino-7,8-dihydro-6-(hydroxymethyl)-7,7-dimethyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

37557-79-2

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37557-79-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 37557-79-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,5,5 and 7 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 37557-79:
(7*3)+(6*7)+(5*5)+(4*5)+(3*7)+(2*7)+(1*9)=152
152 % 10 = 2
So 37557-79-2 is a valid CAS Registry Number.

37557-79-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 7,8-dihydro-6-hydroxymethyl-7,7-dimethylpteridin-4(3H)-one

1.2 Other means of identification

Product number -
Other names 7,8-dihydro-7,7-dimethyl-6-hydroxymethylpterin

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:37557-79-2 SDS

37557-79-2Relevant academic research and scientific papers

Specific Inhibitors in Vitamin Biosynthesis. Part 8. Syntheses of some Functionalised 7,7-Dialkyl-7,8-dihydropterins

Cameron, Robert,Nicholson, Sydney H.,Robinson, David H.,Suckling, Colin J.,Wood, Hamish C. S.

, p. 2133 - 2144 (2007/10/02)

The synthesis of variety of functionalised blocked 7,8-dihydropteridines is described.The functional groups were chosen to provide compounds with potential for investigating the protein chemistry of enzymes in the pathway leading to dihydrofolate and, in particular, of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase.The potential of 7-substituents to provide sites of attachment of inhibitors to columns for affinity chromatography was explored but the extent of the study was curtailed by the restricted applicability of nitrosyl chloride addition to alkenes, a reaction used in the synthesis of pteridine precursors.The syntheses of two compounds, a 6-trichlorophenoxymethyldihydropteridine and of a thiadiazolopteridine, designed to have enchanced transport properties, are also described.

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