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2-Pyrimidinecarboxaldehyde, 4,6-dimethyl- (8CI,9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

27427-90-3

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27427-90-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 27427-90-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,7,4,2 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 27427-90:
(7*2)+(6*7)+(5*4)+(4*2)+(3*7)+(2*9)+(1*0)=123
123 % 10 = 3
So 27427-90-3 is a valid CAS Registry Number.

27427-90-3SDS

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 4,6-dimethylpyrimidine-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 4,6-dimethyl-2-formylpyrimidine

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:27427-90-3 SDS

27427-90-3Relevant academic research and scientific papers

Synthesis and characterization of verdazyl radicals bearing pyridine or pyrimidine substituents: A new family of chelating spin-bearing ligands

Barr, Christa L.,Chase, Preston A.,Hicks, Robin G.,Lemaire, Martin T.,Stevens, Cecilia L.

, p. 8893 - 8897 (1999)

The syntheses and characterization of two new 1,5-dimethyl-6-oxoverdazyl radicals bearing 2-pyridine and 4,6-dimethyl-2-pyrimidine rings as substituents are described. The radical precursors, the corresponding 1,2,4,5-tetrazanes, were prepared by condensa

Studies on Pyrimidine Derivatives. XX. Synthetic Utility of Hydroxymethylpyrimidines and Related Compounds

Sakamoto, Takao,Tanji, Ken-Ichi,Niitsuma, Setsuko,Ono, Takayasu,Yamanaka, Hiroshi

, p. 3362 - 3368 (2007/10/02)

The conversion of a hydroxymethyl group at the 2- or 4-position of simple pyrimidines to a chloromethyl, cyanomethyl, ethoxycarbonylmethyl, or formyl group is described.Various pyrimidines having an olefinic side chain were also synthesized via Witting reagents derived from chloromethylpyrimidines.Keywords - hydroxymethylation; chloromethylpyrimidine; cyanomethylpyrimidine; pyrimidinecarbaldehyde; Witting reaction

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