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3(2H)-Pyridazinone, 6-(4-chlorophenyl)-2-methyl- is a chemical compound belonging to the pyridazinone class, characterized by a pyridazinone ring system with a 4-chlorophenyl group at the 6th position and a methyl group at the 2nd position. 3(2H)-Pyridazinone, 6-(4-chlorophenyl)-2-methyl- has a molecular formula of C10H8ClN3O and a molecular weight of 213.65 g/mol. It is an organic compound with potential applications in pharmaceuticals, agrochemicals, and other chemical industries. Due to its specific structure, it may exhibit unique chemical properties and reactivity, making it a subject of interest for researchers in the field of organic chemistry.

2166-01-0

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2166-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2166-01-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,1,6 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2166-01:
(6*2)+(5*1)+(4*6)+(3*6)+(2*0)+(1*1)=60
60 % 10 = 0
So 2166-01-0 is a valid CAS Registry Number.

2166-01-0SDS

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 6-(4-chlorophenyl)-2-methylpyridazin-3-one

1.2 Other means of identification

Product number -
Other names 6-oxo-1-methyl-3-p-chlorophenyl-1,6-dihydropyridazine

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:2166-01-0 SDS

2166-01-0Downstream Products

2166-01-0Relevant academic research and scientific papers

ALKYLATION OF 6-OXO-1,6-DIHYDROPYRIDAZINES BY TRIETHYLOXONIUM FLUOROBORATE

Volynets, N. F.,Smartseva, I. V.,Khramova, I. V.,Pavlova, L. A.

, p. 1604 - 1608 (2007/10/02)

Irrespective of the nature of the substituents at positions 1 and 3 the heterocycle, 6-oxo-1-phenyl(methyl)-3-aryl-1,6-dihydropyridazines are alkylated by the action of triethyloxonium fluoroborate at the oxygen atom of the carbonyl group, forming heteroaromatic 1-ethoxypyridazinium salts.

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