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947320-08-3

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947320-08-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 947320-08-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,7,3,2 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 947320-08:
(8*9)+(7*4)+(6*7)+(5*3)+(4*2)+(3*0)+(2*0)+(1*8)=173
173 % 10 = 3
So 947320-08-3 is a valid CAS Registry Number.

947320-08-3SDS

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 2-Pyridinecarboxylic acid, 4-(1-methylethyl)-, methyl ester

1.2 Other means of identification

Product number -
Other names 2-Pyridinecarboxylic acid,4-(1-methylethyl)-,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:947320-08-3 SDS

947320-08-3Downstream Products

947320-08-3Relevant academic research and scientific papers

Functionalization of Pyridinium Derivatives with 1,4-Dihydropyridines Enabled by Photoinduced Charge Transfer

Hong, Sungwoo,Kim, Inwon,Park, Seongjin

supporting information, (2020/11/13)

By exploiting electron donor-acceptor (EDA) complexes between 1,4-dihydropyridines and N-amidopyridinium salts under visible light irradiation, we discovered that photoinduced intermolecular charge transfer induces a single-electron transfer event without requiring a photocatalyst for the facile functionalization of pyridines. The generality of this method is amenable to various types of 1,4-dihydropyridines radical precursors to generate structurally different radicals such as alkyl, acyl, and carbamoyl radicals, ultimately providing facile access to synthetically valuable C4-functionalized pyridines. A broad range of functional groups are well accommodated under mild and metal-free conditions, and the synthetic utility of the present method is showcased by the late-stage functionalization of a variety of biologically relevant pyridine-based compounds, pharmaceuticals, and peptide feedstocks.

CYCLIC SULFONES USEFUL AS BACE INHIBITORS

-

Page/Page column 25-26, (2008/06/13)

The invention relates to novel heterocyclic compounds of the formula (I), in which all of the variables are as defined in the specification, in free base form or in acid addition salt form, to their preparation, to their use as medicaments and to medicame

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