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16041-30-8

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16041-30-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 16041-30-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,0,4 and 1 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 16041-30:
(7*1)+(6*6)+(5*0)+(4*4)+(3*1)+(2*3)+(1*0)=68
68 % 10 = 8
So 16041-30-8 is a valid CAS Registry Number.

16041-30-8SDS

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 6-methylpyrazino<2,3-d>pyrimidin-7(8H)-one

1.2 Other means of identification

Product number -
Other names 6-Methyl-8H-pteridin-7-one

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:16041-30-8 SDS

16041-30-8Downstream Products

16041-30-8Relevant articles and documents

Kinetic Study on the Anelation of Heterocycles. 3. Pyrazinopyrimidine Derivatives Synthesized by the Hinsberg Reaction

Abasolo, Maria Ines,Fernandez, Beatriz M.,Magrini, Edgardo

, p. 1279 - 1283 (2007/10/02)

A kinetic study on the obtainment of pyrazinopyrimidine derivatives (pteridines) was performed.The regioselective synthesis of compounds 6-methylpyrazinopyrimidin-7(8H)-one (5a) and 7-methylpyrazinopyrimidin-6(5H)-one (5b), in good yields, was expected by the Hinsberg reaction because the synthesis of both isomers analytically pure was never reported to date.This Hinsberg reaction gave good results to obtain compound 5a, regioselectively and in good yields, either in pH 5 aqueous buffer solution or in methylene chloride, among several organic solvents.However, structural and solvation factors prevented the synthesis of the isomer 5b, which was regioselectively formed in very acid solutions (Ho = -0.89), but in very poor yield.

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