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4-Pyridinecarbonyl chloride, 1,2-dihydro-1-methyl-2-oxo- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84853-99-6

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84853-99-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84853-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,8,5 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 84853-99:
(7*8)+(6*4)+(5*8)+(4*5)+(3*3)+(2*9)+(1*9)=176
176 % 10 = 6
So 84853-99-6 is a valid CAS Registry Number.

84853-99-6SDS

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 1-methyl-2-oxopyridine-4-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 1,2-DIHYDRO-1-METHYL-2-OXO-4-PYRIDINECARBONYL CHLORIDE

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:84853-99-6 SDS

84853-99-6Relevant academic research and scientific papers

SUBSTITUTED PYRAZOLE COMPOUNDS USEFUL AS SOLUBLE EPOXIDE HYDROLASE INHIBITORS

-

Page/Page column 103, (2008/06/13)

Disclosed are compounds active against soluble epoxide hydrolase (sEH), compositions thereof and methods of using and making same.

Substituent Effects in Non-Aromatic Nitrogen Heterocycles: Alkaline Hydrolysis of Methyl N-Methyl(oxo)dihydropyridinecarboxylates and Diaza Analogues

Deady, Leslie W.

, p. 637 - 641 (2007/10/02)

Ester hydrolysis studies on some isomeric methoxycarbonyl derivatives of N-methylpyridin-2- and 4-ones show that reaction rates are affected by the relative positions of CO2Me, =O and NMe functions in ways which could not be predicted.However, from limited results for analogous pyrimidine derivatives, it seems that reactivity in these polyfunctional compounds can be predicted from the pyridine data by assuming additivity of effects.

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