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792136-23-3

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792136-23-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 792136-23-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,9,2,1,3 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 792136-23:
(8*7)+(7*9)+(6*2)+(5*1)+(4*3)+(3*6)+(2*2)+(1*3)=173
173 % 10 = 3
So 792136-23-3 is a valid CAS Registry Number.

792136-23-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1,2,3,6-tetrahydropyridine-4-carboxylate

1.2 Other means of identification

Product number -
Other names 4-pyridinecarboxylic acid,1,2,3,6-tetrahydro-,methyl ester

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:792136-23-3 SDS

792136-23-3Downstream Products

792136-23-3Relevant articles and documents

Palladium-Catalyzed Visible-Light-Driven Carboxylation of Aryl and Alkenyl Triflates by Using Photoredox Catalysts

Shimomaki, Katsuya,Nakajima, Tomoya,Caner, Joaquim,Toriumi, Naoyuki,Iwasawa, Nobuharu

, p. 4486 - 4489 (2019/06/24)

A visible-light-driven carboxylation of aryl and alkenyl triflates with CO2 is developed by using a combination of Pd and photoredox catalysts. This reaction proceeds under mild conditions and can be applied to a wide range of substrates including acyclic alkenyl triflates.

B(C6F5)3-Catalyzed Cascade Reduction of Pyridines

Liu, Zhi-Yun,Wen, Zhi-Hui,Wang, Xiao-Chen

supporting information, p. 5817 - 5820 (2017/05/12)

B(C6F5)3 has been found to be an effective catalyst for reduction of pyridines and other electron-deficient N-heteroarenes with hydrosilanes (or hydroboranes) and amines as the reducing reagents. The success of this development hinges upon the realization of a cascade process of dearomative hydrosilylation (or hydroboration) and transfer hydrogenation. The broad functional-group tolerance (e.g. ketone, ester, unactivated olefins, nitro, nitrile, heterocycles, etc.) implies high practical utility.

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