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3-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.

84854-00-2

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84854-00-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84854-00-2 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 4 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 84854-00:
(7*8)+(6*4)+(5*8)+(4*5)+(3*4)+(2*0)+(1*0)=152
152 % 10 = 2
So 84854-00-2 is a valid CAS Registry Number.

84854-00-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-methyl-2-oxopyridine-3-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 1,2-DIHYDRO-1-METHYL-2-OXO-3-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:84854-00-2 SDS

84854-00-2Relevant academic research and scientific papers

Creation of concave-shaped conformation in crystal structures using an iminodicarbonyl linker. An application to solid-state intramolecular [4 + 4] photocycloaddition reactions of 2-pyridone derivatives

Masu, Hyuma,Ohmori, Ken,Kishikawa, Keiki,Yamamoto, Makoto,Yamaguchi, Kentaro,Kohmoto, Shigeo

, p. 1127 - 1131 (2007/10/03)

Single-crystal X-ray structures of 6 carboxamides possessing two units of 2-pyridone moieties connected with an iminodicarbonyl linker were examined to show the usefulness of this linker for the creation of concave-shaped conformation in crystal structure

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.

A 'Biogenetic Like' Synthesis of Perloline, 6-(3,4-dimethoxyphenyl)-5-hydroxy-5,6-dihydrobenzonaphthyridin-4(3H)-one

Duong, Thach,Prager, Rolf H.,Were, Stephen T.

, p. 1431 - 1440 (2007/10/02)

9H-Indenopyridine-1(2H),9-dione, prepared by a new efficient route, reacts with 3,4-dimethoxyphenyllithium to form the keto alcohol (7), which rearranges with hydrazoic acid to form 5-(3,4-dimethoxyphenyl)benznaphthyridin-4(3H)-one.The N-oxide photolyses smoothly to yield dehydroperloline as the sole product.

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