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2,6-Pyridinedicarboxylic acid, diphenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

10448-12-1

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10448-12-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10448-12-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,4 and 8 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10448-12:
(7*1)+(6*0)+(5*4)+(4*4)+(3*8)+(2*1)+(1*2)=71
71 % 10 = 1
So 10448-12-1 is a valid CAS Registry Number.

10448-12-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name diphenyl pyridine-2,6-dicarboxylate

1.2 Other means of identification

Product number -
Other names Dipicolinsaeure-diphenylester

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:10448-12-1 SDS

10448-12-1Relevant academic research and scientific papers

Palladium-catalyzed carbonylation of aryl, alkenyl, and allyl halides with phenyl formate

Ueda, Tsuyoshi,Konishi, Hideyuki,Manabe, Kei

, p. 3100 - 3103 (2012/07/27)

Highly efficient palladium-catalyzed carbonylation of aryl, alkenyl, and allyl halides with phenyl formate is reported. This procedure does not use carbon monoxide and affords one-carbon-elongated carboxylic acid phenyl esters in excellent yields. The reaction proceeds smoothly under mild conditions and tolerates a wide range of functional groups including aldehyde, ether, ketone, ester, and cyano groups. Furthermore, a variety of heteroaromatic bromides can be converted to the corresponding phenyl esters in high yields.

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