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Ethanone, 1-[2-(methylamino)-5-pyrimidinyl]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

265107-49-1

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265107-49-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 265107-49-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,5,1,0 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 265107-49:
(8*2)+(7*6)+(6*5)+(5*1)+(4*0)+(3*7)+(2*4)+(1*9)=131
131 % 10 = 1
So 265107-49-1 is a valid CAS Registry Number.

265107-49-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[2-(methylamino)pyrimidin-5-yl]ethanone

1.2 Other means of identification

Product number -
Other names Ethanone,1-[2-(methylamino)-5-pyrimidinyl]-

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:265107-49-1 SDS

265107-49-1Downstream Products

265107-49-1Relevant academic research and scientific papers

cGAS ANTAGONIST COMPOUNDS

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Paragraph 0310, (2017/11/06)

Disclosed are novel compounds of Formula (I) that are cGAS antagonists, methods of preparation of the compounds, pharmaceutical compositions comprising the compounds, and their use in medical therapy.

Acetylation of N-heteroaryl bromides via PdCl2/(o-tolyl) 3P catalyzed heck reactions

He, Tianxiong,Tao, Xiaochun,Wu, Xinyan,Cai, Lisheng,Pike, Victor W.

, p. 887 - 890 (2008/09/21)

A new user-friendly and convenient method for the acetylation of N-heteroaryl bromides is described. This process is based on the palladium-catalyzed olefination of an N-heteroaryl bromide with butyl vinyl ether, followed by acid hydrolysis of the intermediate heteroaryl vinyl ether in situ. Isopropanol at 85°C, in the presence of K3PO 4·3H2O (2 equiv), PdCl2 (2 mol%) and (o-tolyl)3P (4 mol%), provided the best conditions, giving yields of N-heteroaryl bromides up to 75%. Georg Thieme Verlag Stuttgart.

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