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69491-43-6

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69491-43-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 69491-43-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,4,9 and 1 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69491-43:
(7*6)+(6*9)+(5*4)+(4*9)+(3*1)+(2*4)+(1*3)=166
166 % 10 = 6
So 69491-43-6 is a valid CAS Registry Number.

69491-43-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3-methoxyphenyl) pyrimidine

1.2 Other means of identification

Product number -
Other names 2-(3-methoxy-phenyl)-pyrimidine

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:69491-43-6 SDS

69491-43-6Relevant articles and documents

Cyclometallated 2-Phenylpyrimidine Derived Platinum Complexes: Synthesis and Photophysical Properties

Fecková, Michaela,Kahlal, Samia,Roisnel, Thierry,Saillard, Jean-Yves,Boixel, Julien,Hruzd, Mariia,le Poul, Pascal,Gauthier, Sébastien,Robin-le Guen, Fran?oise,Bure?, Filip,Achelle, Sylvain

, p. 1592 - 1600 (2021)

A series of five platinum (II) complexes based on 2-phenylpyrimidine ligands have been designed. Pyridine and chloride were used as auxiliary ligands. These complexes exhibit a slightly distorted square-planar geometry. The nature and position of substitu

Small-molecule pyrimidine inhibitors of the cdc2-like (Clk) and dual specificity tyrosine phosphorylation-regulated (Dyrk) kinases: Development of chemical probe ML315

Coombs, Thomas C.,Tanega, Cordelle,Shen, Min,Wang, Jenna L.,Auld, Douglas S.,Gerritz, Samuel W.,Schoenen, Frank J.,Thomas, Craig J.,Aubé, Jeffrey

supporting information, p. 3654 - 3661 (2013/07/05)

Substituted pyrimidine inhibitors of the Clk and Dyrk kinases have been developed, exploring structure-activity relationships around four different chemotypes. The most potent compounds have low-nanomolar inhibitory activity against Clk1, Clk2, Clk4, Dyrk

Palladium-Catalyzed Regioselective C-H Bond ortho-Acetoxylation of Arylpyrimidines

Zheng, Xiaojian,Song, Bingrui,Xu, Bin

supporting information; experimental part, p. 4376 - 4380 (2010/10/04)

An efficient and regioselective palladium-catalyzed ortho C-H acetoxylation reaction was developed to afford, ortho monoacetoxylated arylpyrimidmes in good to excellent yields by using cupric trifluoroacetate as a cocatalyst. A wide variety of oxygenated

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