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835-09-6

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835-09-6 Usage

Description

(2-bromo-5-chlorophenyl)(phenyl)methanone, also known as Bromochlorophenylphenylketone, is a chemical compound with the molecular formula C13H8BrClO. It is a white to off-white solid that is insoluble in water but soluble in organic solvents. (2-bromo-5-chlorophenyl)(phenyl)methanone is a versatile building block for the synthesis of a wide range of bioactive compounds, making it a valuable reagent in the pharmaceutical industry.

Uses

Used in Organic Synthesis:
(2-bromo-5-chlorophenyl)(phenyl)methanone is used as a versatile intermediate for the synthesis of various organic compounds. Its unique structure allows for the creation of a wide range of molecules with potential applications in different industries.
Used in Pharmaceutical Research:
(2-bromo-5-chlorophenyl)(phenyl)methanone is used as a key building block in the development of new pharmaceuticals. Its presence in the molecular structure can contribute to the desired biological activity of the final product, making it an essential component in drug discovery and design.
Used in Agrochemical Production:
(2-bromo-5-chlorophenyl)(phenyl)methanone is used as an intermediate in the production of various agrochemicals. Its chemical properties make it suitable for the synthesis of compounds that can be used in agriculture to protect crops and enhance yield.
It is important to handle (2-bromo-5-chlorophenyl)(phenyl)methanone with proper safety precautions due to its potential hazards.

Check Digit Verification of cas no

The CAS Registry Mumber 835-09-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,3 and 5 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 835-09:
(5*8)+(4*3)+(3*5)+(2*0)+(1*9)=76
76 % 10 = 6
So 835-09-6 is a valid CAS Registry Number.

835-09-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name (2-bromo-5-chlorophenyl)-phenylmethanone

1.2 Other means of identification

Product number -
Other names 2-benzoyl-4-chloro-1-bromobenzene

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:835-09-6 SDS

835-09-6Relevant articles and documents

Palladium(II)-catalyzed Intermolecular Cascade Cyclization of Methylenecyclopropanes with Aromatic Alkynes: Construction of Spirocyclic Compounds Containing Indene and 1,2-Dihydronaphthalene Moieties

Fang, Wei,Wei, Yin,Shi, Min

, (2019/05/22)

A palladium(II)-catalyzed intermolecular cascade cyclization of methylenecyclopropanes with aromatic alkynes is reported in this paper. The reaction involves a migratory insertion of alkyne, an intramolecular Heck-type reaction, and β-H elimination, providing a series of spirocyclic compounds containing indene and 1,2-dihydronaphthalene moieties in moderate to excellent yields upon heating.

Synthesis of 3-aryl-2-methoxyinden-1-one (Z)-phenylhydrazones via hydrobromic acid-mediated cyclization of 2-(1-aryl-2-methoxyethenyl)benzaldehyde phenylhydrazones

Kobayashi, Kazuhiro,Miyatani, Wataru,Matsumoto, Naoki

, p. 239 - 245 (2013/03/28)

2-(1-Aryl-2-methoxyethenyl)benzaldehydes 2, obtained by successive treatment of 1-(1-aryl-2-methoxyethenyl)-2-bromobenzenes 1 with BuLi and 1-formylpiperidine, were transformed to the corresponding phenylhydrazones 3 on treatment with PhNHNH2.

1-ARYL-4-SUBSTITUTED PIPERAZINES DERIVATIVES FOR USE AS CCR1 ANTAGONISTS FOR THE TREATMENT OF INFLAMMATION AND IMMUNE DISORDERS

-

Page 58-59, (2008/06/13)

Compounds are provided that act as potent antagonists of the CCR1 receptor, and which have been further confirmed in animal testing for inflammation, one of the hallmark disease states for CCR1. The compounds are generally aryl piperazine derivatives and are useful in pharmaceutical compositions, methods for the treatment of CCR1-mediated diseases, and as controls in assays for the identification of competitive CCR1 antagonists.

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