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10-ethyldibenzo[b,f][1,4]oxazepin-11(10H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

17296-50-3

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17296-50-3 Usage

Chemical structure

Tricyclic dibenzazepine derivative with a nitrogen-containing seven-membered heterocycle

Application

Pharmaceutical intermediate in the synthesis of drugs for psychiatric and neurological disorders

Pharmacological effects

Sedative, anxiolytic, and antipsychotic properties

Potential treatment

Mood disorders such as depression and anxiety

Risks and side effects

Potential risks and side effects, should be used under the supervision of a qualified healthcare professional

Usage

Commonly used in the pharmaceutical industry

Chemical class

Heterocyclic compound

Check Digit Verification of cas no

The CAS Registry Mumber 17296-50-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,2,9 and 6 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 17296-50:
(7*1)+(6*7)+(5*2)+(4*9)+(3*6)+(2*5)+(1*0)=123
123 % 10 = 3
So 17296-50-3 is a valid CAS Registry Number.

17296-50-3SDS

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 5-ethylbenzo[b][1,4]benzoxazepin-6-one

1.2 Other means of identification

Product number -
Other names Dibenzoxazepinone 10

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:17296-50-3 SDS

17296-50-3Downstream Products

17296-50-3Relevant academic research and scientific papers

Regioselective synthesis of fused oxazepinone scaffolds through one-pot smiles rearrangement tandem reaction

Liu, Yanli,Chu, Chunxiao,Huang, Aiping,Zhan, Chunjing,Ma, Ying,Ma, Chen

experimental part, p. 547 - 553 (2011/10/18)

The paper describes a convenient and facile methodology for the regioselective synthesis of fused oxazepinone scaffolds. This process is an efficient construction of the oxazepinone scaffold by a one-pot coupling/Smiles rearrangement/cyclization approach.

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