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70415-72-4

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70415-72-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 70415-72-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,0,4,1 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 70415-72:
(7*7)+(6*0)+(5*4)+(4*1)+(3*5)+(2*7)+(1*2)=104
104 % 10 = 4
So 70415-72-4 is a valid CAS Registry Number.

70415-72-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-methoxybenzoic acid 2-pyridinylmethyl ester

1.2 Other means of identification

Product number -
Other names p-Methoxy-benzoesaeure-2-picolylester

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:70415-72-4 SDS

70415-72-4Relevant articles and documents

Nickel-catalyzed alkoxycarbonylation of aryl iodides with 1 atm CO

Liu, Ning,Wu, Xianqing,Wang, Chenglong,Qu, Jingping,Chen, Yifeng

supporting information, p. 4643 - 4646 (2022/04/19)

A nickel-catalyzed alkoxycarbonylation of aromatic iodides with alcohols under atmospheric pressure of carbon monoxide is presented here. This operationally simple protocol allows the facile synthesis of (hetero)aromatic esters, exhibiting broad substrate scope with excellent functional group tolerance. Various primary and secondary aliphatic alcohols as well as phenols are suitable for this transformation.

Practical: In situ -generation of phosphinite ligands for palladium-catalyzed carbonylation of (hetero)aryl bromides forming esters

Wang, Lin,Neumann, Helfried,Spannenberg, Anke,Beller, Matthias

, p. 7469 - 7472 (2017/07/12)

An effective method for alkoxycarbonylation of (hetero)aryl bromides is developed in the presence of in situ-generated phosphinite ligands tBu2POR (R = nBu, nPr, Et or Me). For this purpose commercially available tBu2PCl was used as the pre-ligand in the presence of different alcohols. For the first time cross coupling reactions with two alcohols-one generating the ligand, the other used as substrate-were developed. Through this method, ligand optimization can be performed in a more efficient manner and the desired products could be obtained with good yields and selectivity.

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