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6128-06-9

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6128-06-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6128-06-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,2 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 6128-06:
(6*6)+(5*1)+(4*2)+(3*8)+(2*0)+(1*6)=79
79 % 10 = 9
So 6128-06-9 is a valid CAS Registry Number.

6128-06-9SDS

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 4-methoxy-1H-pyrimidin-6-one

1.2 Other means of identification

Product number -
Other names 6-Methoxy-4-oxo-3,4-dihydro-pyrimidin

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:6128-06-9 SDS

6128-06-9Downstream Products

6128-06-9Relevant articles and documents

-

Katritzky et al.

, p. 562 (1966)

-

Novel procedure for selective C-nitrosation of aminopyrimidine derivatives under neutral conditions. Scope and synthetic applications

Marchal, Antonio,Melguizo, Manuel,Nogueras, Manuel,Sánchez, Adolfo,Low, John N.

, p. 255 - 258 (2007/10/03)

A novel simple method, based on treatment with isoamyl nitrite (IAN) in DMSO without any added acid, to produce selective C(5)-nitrosation of aminopyrimidine derivatives is described. It proved to be suitable for a multigram scale and applicable to a larger range of pyrimidine derivatives, including amino-dialkoxypyrimidines, than the procedures previously known. Its scope is analyzed and some example on the usefulness of the newly prepared substances as intermediates in the synthesis of fused heterobicyclic derivatives of potential biological interest is presented.

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