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124392-61-6

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124392-61-6 Usage

General Description

(4Z)-4-[(4-chlorophenyl)methylidene]-7-methyl-3,4-dihydro-1-benzoxepin-5(2H)-one is a chemical compound with a complex molecular structure. It contains a benzoxepin ring and a phenyl group, as well as a double bond in its side chain. The chlorophenyl group adds a chlorine atom to the phenyl ring, giving the compound its distinct properties. This chemical may have potential pharmaceutical applications due to its unique structure and properties, and further research may be needed to investigate its potential uses. Additionally, its chemical properties and reactivity could make it useful for a wide range of industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 124392-61-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,3,9 and 2 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124392-61:
(8*1)+(7*2)+(6*4)+(5*3)+(4*9)+(3*2)+(2*6)+(1*1)=116
116 % 10 = 6
So 124392-61-6 is a valid CAS Registry Number.

124392-61-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (4Z)-4-[(4-chlorophenyl)methylidene]-7-methyl-2,3-dihydro-1-benzoxepin-5-one

1.2 Other means of identification

Product number -
Other names 1-Benzoxepin-5(2H)-one,3,4-dihydro-4-((4-chlorophenyl)methylene)-7-methyl

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:124392-61-6 SDS

124392-61-6Relevant articles and documents

Synthesis and Biological Activities of 8,9-Disubstituted 4,5-Dihydro-2H--benzoxepinopyrazoles and Related Compounds

Tripathi, Ravish C.,Tandon, V. K.,Khanna, J. M.,Saxena, Anil K.,Anand, Nitya

, p. 37 - 41 (2007/10/02)

Condensation of 2,3,4,5-tetrahydro-1-benzoxepin-5-ones (2a-d) with different benzaldehydes affords the benzylidine derivatives (3a-d) which on epoxidation followed by treatment with hydrazine hydrate and arylhydrazines furnish the title benzoxepinopyrazol

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