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Pyridine, 3-chloro-2,6-diphenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91404-09-0

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91404-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91404-09-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,4,0 and 4 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 91404-09:
(7*9)+(6*1)+(5*4)+(4*0)+(3*4)+(2*0)+(1*9)=110
110 % 10 = 0
So 91404-09-0 is a valid CAS Registry Number.

91404-09-0SDS

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 3-chloro-2,6-diphenylpyridine

1.2 Other means of identification

Product number -
Other names Pyridine,3-chloro-2,6-diphenyl

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:91404-09-0 SDS

91404-09-0Downstream Products

91404-09-0Relevant articles and documents

REACTION OF α-α'-DICHLORO-SUBSTITUTED 1,5-DIKETONES WITH AMMONIA AND AMMONIUM ACETATE

Kharchenko, V. G.,Chalaya, S. N.,Litvinov, O. V.

, p. 291 - 293 (1985)

Under the influence of ammonia or ammonium acetate, α-α'-dichloro-substituted 1,5-diketones undergo heterocyclization to give β-chloropyridines or 2-benzoylpyrrole derivatives.The structure of the final product depends on the reagent and the character of

CYCLIZATION OF 2,4-DICHLORO-1,5-PENTANEDIONES WITH NUCLEOPHILIC REAGENTS

Litvinov, O. V.,Chalaya, S. N.,Kharchenko, V. G.

, p. 878 - 882 (2007/10/02)

The mechanism of reaction of 2,4-dichloro-1,5-pentanediones with ammonia has been studied.Intramolecular cyclization of the intermediate resulting from nucleophilic attack at the carbonyl group can occur in two ways, depending on the reaction conditions,

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