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

50345-29-4

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50345-29-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50345-29-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,4 and 5 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 50345-29:
(7*5)+(6*0)+(5*3)+(4*4)+(3*5)+(2*2)+(1*9)=94
94 % 10 = 4
So 50345-29-4 is a valid CAS Registry Number.

50345-29-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name [6-(hydroxymethyl)pyrimidin-4-yl]methanol

1.2 Other means of identification

Product number -
Other names 4,6-PYRIMIDINEDIMETHANOL

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:50345-29-4 SDS

50345-29-4Downstream Products

50345-29-4Relevant academic research and scientific papers

Hydroxymethylations of aryl halides by Pd-catalyzed cross-couplings with (benzoyloxy)methylzinc iodide - Scope and limitations of the reaction

Hasník, Zbyněk,?ilhár, Peter,Hocek, Michal

, p. 543 - 546 (2008/12/22)

Palladium-catalyzed cross-coupling reactions of (benzoyloxymethyl)zinc iodide with diverse (het)aryl halides leading to (benzoyloxymethyl)(het)arenes were studied to define the scope of this reaction. It has been found that this reaction is only applicable for electron-deficient aryl halides and the most efficient it is for 2-halopyridines and 4-halopyrimidines. Deprotection of the intermediates gives (hydroxymethyl)pyridines and -pyrimidines in high yields. Georg Thieme Verlag Stuttgart.

PHARMACOLOGICALLY ACTIVE THIOUREA AND UREA COMPOUNDS

-

, (2008/06/13)

The compounds are substituted thioalkyl-, aminoalkyl-and oxyalkyl-thioureas and ureas which are inhibitors of histamine activity.

PHARMACOLOGICALLY ACTIVE GUANIDINE COMPOUNDS

-

, (2008/06/13)

The compounds are substituted thioalkyl-, aminoalkyl-and oxyalkyl-guanidines which are inhibitors of histamine activity.

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