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2165-04-0

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2165-04-0 Usage

Description

2-METHYL-6-PHENYLPYRIDAZIN-3(2H)-ONE, a pyridazinone derivative with the molecular formula C11H10N2O, is a chemical compound that features a heterocyclic ring composed of carbon, nitrogen, and oxygen atoms. This unique structure endows it with distinctive properties, making it a versatile compound with potential applications in pharmaceuticals, agriculture, and organic synthesis.

Uses

Used in Pharmaceutical Industry:
2-METHYL-6-PHENYLPYRIDAZIN-3(2H)-ONE is used as an antiproliferative agent for its potential to inhibit the growth of certain types of cells, which can be beneficial in the development of treatments for various diseases, including cancer.
Used in Agricultural Industry:
2-METHYL-6-PHENYLPYRIDAZIN-3(2H)-ONE is used as an antibacterial agent, leveraging its ability to combat bacterial growth, which can be advantageous in the development of new pesticides or antimicrobial agents for crop protection.
Used in Organic Synthesis:
2-METHYL-6-PHENYLPYRIDAZIN-3(2H)-ONE is used as a building block in organic synthesis, contributing to the creation of new compounds with diverse applications in various fields, such as pharmaceuticals, materials science, and chemical research. Its unique heterocyclic structure allows for the development of novel molecules with potential therapeutic or industrial uses.

Check Digit Verification of cas no

The CAS Registry Mumber 2165-04-0 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 5 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2165-04:
(6*2)+(5*1)+(4*6)+(3*5)+(2*0)+(1*4)=60
60 % 10 = 0
So 2165-04-0 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O/c1-13-11(14)8-7-10(12-13)9-5-3-2-4-6-9/h2-8H,1H3

2165-04-0SDS

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 2-methyl-6-phenylpyridazin-3-one

1.2 Other means of identification

Product number -
Other names 2-Methyl-6-phenyl-2H-pyridazin-3-on

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:2165-04-0 SDS

2165-04-0Relevant articles and documents

Copper-catalyzed aerobic dehydrogenation of C-C to C=C bonds in the synthesis of pyridazinones

Liang, Lei,Yang, Guanyu,Xu, Fengrong,Niu, Yan,Sun, Qi,Xu, Ping

supporting information, p. 6130 - 6136 (2013/09/24)

A simple and efficient procedure for the synthesis of pyridazin-3(2H)-ones through copper-catalyzed dehydrogenation of a single C-C bond of 4,5-dihydropyridazin-3(2H)-ones to a C=C bond with oxygen as the terminal oxidant is described. Functional groups including hydroxy, carboxylic, bromo, chloro, cyano, nitro and alkoxy were all tolerated under the reaction conditions. Moreover, this methodology was applied to the preparation of a series of structurally similar N-substituted 6-phenylpyridazinone compounds containing fluorine. The dehydrogenation reactions exhibit good yields and selectivity. Copper-catalyzed dehydrogenation of a C-C bond of 4,5-dihydropyridazinones to a C=C bond with oxygen as the terminal oxidant is described. Various functional groups were tolerated under the reaction conditions. The method was also applied to the preparation of a series of N-substituted 6-phenylpyridazinones containing fluoride. The dehydrogenation reactions exhibit good yields and selectivity.

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.

ALKYLATION OF 1,3-DISUBSTITUTED 60OXODIHYDROPYRIDAZINES

Volynets, N. F.,Samartseva, I. V.,Pavlova, L. A.

, p. 1365 - 1366 (2007/10/02)

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