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Dibenz[c,e]oxepin, 5,7-dihydro- is a chemical compound belonging to the class of dibenzoxepines, which are tricyclic aromatic compounds consisting of two benzene rings fused to an oxepine ring. This specific compound has a molecular formula of C13H10O and a molecular weight of 182.22 g/mol. It is characterized by the presence of a dihydro group, which means it has two hydrogen atoms added to the parent compound. Dibenz[c,e]oxepin, 5,7-dihydro- is an organic compound with potential applications in the pharmaceutical and chemical industries, particularly in the synthesis of various drugs and other organic compounds. Its structure and properties make it an interesting target for further research and development in the field of organic chemistry.

1136-22-7

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1136-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1136-22-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,3 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1136-22:
(6*1)+(5*1)+(4*3)+(3*6)+(2*2)+(1*2)=47
47 % 10 = 7
So 1136-22-7 is a valid CAS Registry Number.

1136-22-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6,7-dihydro-5H-dibenz[c,e]oxepine

1.2 Other means of identification

Product number -
Other names .5,7-dihydro-dibenzo[c,e]oxepine

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:1136-22-7 SDS

1136-22-7Relevant academic research and scientific papers

Synthesis of biphenyl-based ligand: Application in copper-mediated chemoselective michael reaction

Sundar, M. Shyam,Bedekar, Ashutosh V.

, p. 3582 - 3593 (2014)

A biphenyl-based ligand attached was synthesized and screened in copper-mediated Michael reaction. The catalyst system works well with carbon or sulfur nucleophiles as Michael donors and cyclohexenone or chalcones as the acceptors under mild and neutral r

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