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71653-37-7

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71653-37-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71653-37-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,6,5 and 3 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 71653-37:
(7*7)+(6*1)+(5*6)+(4*5)+(3*3)+(2*3)+(1*7)=127
127 % 10 = 7
So 71653-37-7 is a valid CAS Registry Number.

71653-37-7SDS

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 pyridine-2-carboxylic acid benzyl ester

1.2 Other means of identification

Product number -
Other names Picolinsaeurebenzylester

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:71653-37-7 SDS

71653-37-7Relevant articles and documents

A solvent-reagent selection guide for Steglich-type esterification of carboxylic acids

Jordan, Andrew,Sneddon, Helen F.,Sydenham, Jack,Whymark, Kyran D.

supporting information, p. 6405 - 6413 (2021/09/10)

The Steglich esterification is a widely employed method for the formation of esters under mild conditions. A number of issues regarding the sustainability of this transformation have been identified, chiefly the use of hazardous carbodiimide coupling reagents in conjunction with solvents with considerable issues such as dichloromethane (DCM) and N,N-dimethylformamide (DMF). To overcome these issues, we have developed a solvent-reagent selection guide for the formation of esters via Steglich-type reactions with the aim of providing safer, more sustainable conditions. Optimum reaction conditions have been identified after high-throughput screening of solvent-reagent combinations, namely the use of Mukaiyama's reagent (Muk) in conjunction with solvent dimethyl carbonate (DMC). The new reaction conditions were also exemplified through the synthesis of a small selection of building-block like molecules and includes the formation of t-butyl esters.

Picolinate-Directed Arene meta-C-H Amination via FeCl3 Catalysis

Anugu, Raghunath Reddy,Falck, John R.,Munnuri, Sailu

supporting information, p. 5266 - 5271 (2020/04/08)

Direct C-H functionalization of aromatic compounds is a powerful tool for organic synthesis; however, differentiation among the ubiquitous and often chemically similar C-H bonds remains a significant challenge. Conflation with coordinating or directing groups incorporated into the intended substrate has helped address these limitations, although access to remote sites remains limited. Herein, we report an operationally simple and sustainable direct meta-selective H2N amination of benzylic and related aromatic picolinates under conditions mild enough to modify polyfunctional and late-stage molecules.

Thorium complexes possessing expanded ring N-heterocyclic iminato ligands: Synthesis and applications

Ghatak, Tapas,Drucker, Shani,Fridman, Natalia,Eisen, Moris S.

supporting information, p. 12005 - 12009 (2017/09/25)

Six and seven membered N-heterocyclic iminato ligands (L) are introduced allowing access a new class of Th(iv) complexes of the type Cp?2Th(L)(CH3). These complexes were studied in the Tishchenko reaction. Stoichiometric reactions together with kinetic and thermodynamic studies permit us to propose a plausible mechanism.

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