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353497-31-1

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353497-31-1 Usage

Chemical class

Dibenzoazepines

Explanation

It belongs to a class of tricyclic compounds with a seven-membered ring fused to two benzene rings.

Explanation

The compound is derived from the parent compound dibenzoazepine.

Explanation

The methyl ester form of the compound is widely used as an intermediate in the synthesis of various drugs.

Explanation

Drugs synthesized using this compound may have effects on the central nervous system.

Explanation

The compound has been researched for its possible therapeutic effects in treating mental health conditions such as depression and anxiety.

Explanation

The compound may be used as a starting material for the synthesis of other chemical compounds in the field of organic chemistry.

Explanation

The compound has a specific chemical structure that defines its properties and potential applications.

Explanation

The molecular formula represents the number of carbon, hydrogen, nitrogen, and oxygen atoms in the compound.

Explanation

The molecular weight is an important property that can influence the compound's physical and chemical behavior.

Explanation

The solubility of the compound in various solvents is not provided, but it is an important property for its use in pharmaceutical synthesis and organic chemistry.

Derivation

Derived from dibenzoazepine

Methyl ester derivative

Commonly used in the pharmaceutical industry

Central nervous system activity

Synthesized drugs have potential applications

Therapeutic effects

Studied for potential use in depression and anxiety disorders

Organic synthesis

Potential applications in the production of other chemical compounds

Chemical structure

10,11-Dihydro-10-oxo-5H-dibenzo[b,f]azepine-5-carboxylic acid methyl ester

Molecular weight

Approximately 293.33 g/mol (calculated from the molecular formula)

Solubility

Not mentioned in the material

Check Digit Verification of cas no

The CAS Registry Mumber 353497-31-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,5,3,4,9 and 7 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 353497-31:
(8*3)+(7*5)+(6*3)+(5*4)+(4*9)+(3*7)+(2*3)+(1*1)=161
161 % 10 = 1
So 353497-31-1 is a valid CAS Registry Number.

353497-31-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name Methyl 10-oxo-10,11-dihydro-5H-dibenzo[b,f]azepine-5-carboxylate

1.2 Other means of identification

Product number -
Other names 5H-Dibenz[b,f]azepine-5-carbonitrile,10,11-dihydro-10-oxo

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:353497-31-1 SDS

353497-31-1Relevant articles and documents

A new industrial process for oxcarbazepine

Fuenfschilling, Peter C.,Zaugg, Werner,Beutler, Ulrich,Kaufmann, Daniel,Lohse, Olivier,Mutz, Jean-Paul,Onken, Ulrich,Reber, Jean-Louis,Shenton, David

, p. 272 - 277 (2012/12/24)

A novel industrial process for the antiepileptic drug oxcarbazepine 1 has been developed. Unlike the old process, the new process is free from halogenated solvents and can be performed in standard production equipment. It starts from commercially available 1,3-dihydro-1-phenyl-2H-indol-2-one 10. In the key step, an electrophilic ring closure reaction of 2-[(methoxycarbonyl)phenylamino] benzeneacetic acid 5 to 10,11-dihydro-10-oxo-5H-dibenz[b,f]azepine-5-carboxylic acid methyl ester 6 in poly phosphoric acid was applied. For the manufacture of 5, a highly efficient process using a dianion strategy was developed.

Dibenzo(b,f)azepine derivatives and their preparation

-

, (2008/06/13)

The invention relates to new processes for the preparation of the pharmaceutical oxcarbazepine, as well as novel intermediates prepared by or used for said processes, and the preparation of said intermediates.

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