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Methyl 6-Methyl-4-(p-tolyl)picolinate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1338441-77-2

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1338441-77-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1338441-77-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,3,8,4,4 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1338441-77:
(9*1)+(8*3)+(7*3)+(6*8)+(5*4)+(4*4)+(3*1)+(2*7)+(1*7)=162
162 % 10 = 2
So 1338441-77-2 is a valid CAS Registry Number.

1338441-77-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 6-methyl-4-(4-methylphenyl)pyridine-2-carboxylate

1.2 Other means of identification

Product number -
Other names Methyl 6-methyl-4-(p-tolyl)picolinate

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:1338441-77-2 SDS

1338441-77-2Downstream Products

1338441-77-2Relevant academic research and scientific papers

Palladium(II)-Catalyzed Substituted Pyridine Synthesis from ?±,?-Unsaturated Oxime Ethers via a C-H Alkenylation/Aza-6?-Electrocyclization Approach

Yamada, Takahiro,Hashimoto, Yoshimitsu,Tanaka, Kosaku,Morita, Nobuyoshi,Tamura, Osamu

, p. 1659 - 1663 (2021/03/03)

An efficient synthetic method for multisubstituted pyridines from β-aryl-substituted α,β-unsaturated oxime ethers and alkenes via Pd-catalyzed C-H activation has been developed. Systematic optimization of catalyst ligands revealed that sterically hindered

Synthesis of 2,4,6-trisubstituted pyridines via an olefin cross-metathesis/Heck-cyclisation-elimination sequence

Donohoe, Timothy J.,Bower, John F.,Baker, David B.,Basutto, Jose A.,Chan, Louis K. M.,Gallagher, Peter

, p. 10611 - 10613 (2011/11/04)

Heck reactions were performed on α,β-unsaturated-δ- sulfonamido intermediates, derived from cross metathesis, to allow the instalment of substituents at the β position. Subsequent one-pot cyclisation/elimination provides an operationally simple, catalytic and convergent synthesis of 2,4,6-trisubstituted pyridines.

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