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25961-11-9

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25961-11-9 Usage

Description

5-Acetyl-3-chloro-10,11-dihydro-5H-dibenz[b,f]azepine is an organic compound with a complex chemical structure, characterized by its dibenzazepine core, a chlorine atom at the 3-position, and an acetyl group at the 5-position. 5-Acetyl-3-chloro-10,11-dihydro-5H-dibenz[b,f]azepine is known for its potential applications in various chemical and pharmaceutical processes due to its unique structural features.

Uses

Used in Pharmaceutical Industry:
5-Acetyl-3-chloro-10,11-dihydro-5H-dibenz[b,f]azepine is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a key component in the development of new drugs with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of organic chemistry, 5-Acetyl-3-chloro-10,11-dihydro-5H-dibenz[b,f]azepine is used as a reactant in various syntheses. Its versatility in chemical reactions makes it a valuable building block for creating a wide range of complex organic molecules.
Used in the Synthesis of Carbamazepine Impurity 1:
5-Acetyl-3-chloro-10,11-dihydro-5H-dibenz[b,f]azepine is specifically used in the synthesis of Carbamazepine Impurity 1, which is an important compound in the pharmaceutical industry. This application highlights the compound's role in the development of specific drug impurities, which can be crucial for understanding drug behavior and safety.
Used in the Synthesis of Solid Pyridylzinc Reagents:
5-Acetyl-3-chloro-10,11-dihydro-5H-dibenz[b,f]azepine is also used in the synthesis of solid pyridylzinc reagents, which have applications in Negishi Reactions. These reactions are important in the field of organic chemistry, as they allow for the formation of carbon-carbon and carbon-heteroatom bonds, leading to the creation of a diverse range of organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 25961-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,6 and 1 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25961-11:
(7*2)+(6*5)+(5*9)+(4*6)+(3*1)+(2*1)+(1*1)=119
119 % 10 = 9
So 25961-11-9 is a valid CAS Registry Number.
InChI:InChI=1/C16H14ClNO/c1-11(19)18-15-5-3-2-4-12(15)6-7-13-8-9-14(17)10-16(13)18/h2-5,8-10H,6-7H2,1H3

25961-11-9SDS

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 1-(2-chloro-5,6-dihydrobenzo[b][1]benzazepin-11-yl)ethanone

1.2 Other means of identification

Product number -
Other names 3-Chloro-5-acetyliminodibenzyl

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:25961-11-9 SDS

25961-11-9Relevant articles and documents

LIPOXYGENASE INHIBITORS

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Paragraph 00545-00547, (2021/10/02)

Various embodiments of the present disclosure are directed to compounds having Formula (I), Formula (IA), Formula (IB), Formula (IC), Formula (ID), Formula (IE), and/or pharmaceutically acceptable salts thereof. The compounds can be suitable for inhibiting lipoxygenases, and/or treating associated diseases, such as Alzheimer's disease. In some embodiments, the compounds may be administered to a patient as part of a pharmaceutical formulation.

An improved method for the preparation of 3-substituted 10,11-dihydro-5H-[b,f] azepine derivatives

Csende, Ferenc,Hosztafi, Sándor

, p. 587 - 589 (2007/10/03)

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