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Ethenamine, N,N-dimethyl-2-5-nitro-2,6-bis(phenylmethoxy)-4-pyrimidinyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

222631-55-2

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222631-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 222631-55-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,2,6,3 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 222631-55:
(8*2)+(7*2)+(6*2)+(5*6)+(4*3)+(3*1)+(2*5)+(1*5)=102
102 % 10 = 2
So 222631-55-2 is a valid CAS Registry Number.

222631-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4-bis-O-benzyl-5-nitro-6-β-dimethylaminovinylpyrimidine

1.2 Other means of identification

Product number -
Other names 2,4-dibenzyloxy-6-(2-dimethylaminoethenyl)-5-nitropyrimidine

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:222631-55-2 SDS

222631-55-2Relevant academic research and scientific papers

THIENO- AND PYRROLOPYRIMIDINE ANALOGUES AS ANTICANCER AGENTS AND METHODS OF USE THEREOF

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Paragraph 0073-0074, (2016/09/26)

The present invention provides for the design and synthesis of halogenated thieno- and pyrrolopyrimidine compounds that exhibit cancer proliferation inhibitory activity and the use thereof for cancer treatment.

Antiproliferative activities of halogenated pyrrolo[3,2-d]pyrimidines

Temburnikar, Kartik W.,Ross, Christina R.,Wilson, Gerald M.,Balzarini, Jan,Cawrse, Brian M.,Seley-Radtke, Katherine L.

, p. 4354 - 4363 (2015/08/03)

In vitro evaluation of the halogenated pyrrolo[3,2-d]pyrimidines identified antiproliferative activities in compounds 1 and 2 against four different cancer cell lines. Upon screening of a series of pyrrolo[3,2-d]pyrimidines, the 2,4-Cl compound 1 was foun

Process for preparing 2-pyrrolidinyl-1H-pyrrolo[3,2-d]pyrimidine inhibitors of nucleoside metabolism

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Page column 19, (2008/06/13)

A process of preparing a compound of the formula (I) wherein B is chosen from OH, NH2, NHR, H or halogen; D is chosen from OH, NH2, NHR, H halogen or SCH3; R is an optionally substituted alkyl, aralkyl or aryl group; and Z is selected from OH, hydrogen, halogen, hydroxy, SQ or OQ, Q is an optionally substituted all, aralkyl or aryl group; or a tautomer thereof; or a pharmaceutically acceptable salt thereof; or an ester thereof; or a prodrug thereof, which comprises reacting a compound of the formula (II) ?with an anion produced by abstraction of the bromine or iodine atom from a compound of formula (XIX), ?to form a compound of formula (XX) The compound of formula (XX) is N- and O-deprotected to obtain the compound of formula (I).

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