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1208-76-0

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1208-76-0 Usage

General Description

1-BENZYL-4-OXOAZEPANE HCL is a chemical compound that belongs to the azepane class. It is a hydrochloride salt form of the compound and is used in the synthesis of pharmaceutical products. 1-BENZYL-4-OXOAZEPANE HCL has potential use as a psychiatric drug due to its effects on the central nervous system. It is also used in research and development as a building block for the creation of novel molecules with potential therapeutic applications. 1-BENZYL-4-OXOAZEPANE HCL is an important intermediate in organic synthesis and is commonly utilized in pharmaceutical and chemical industries.

Check Digit Verification of cas no

The CAS Registry Mumber 1208-76-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,0 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1208-76:
(6*1)+(5*2)+(4*0)+(3*8)+(2*7)+(1*6)=60
60 % 10 = 0
So 1208-76-0 is a valid CAS Registry Number.

1208-76-0SDS

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 1-benzylazepan-4-one,hydrochloride

1.2 Other means of identification

Product number -
Other names hexahydro-1-(phenylmethyl)-4H-azepin-4-one hydrochloride

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:1208-76-0 SDS

1208-76-0Relevant articles and documents

Method for the preparation of hexahydroazepinones and hexahydroazepinoles

-

, (2008/06/13)

This disclosure describes two technical procedures for the high-yield synthesis of heterocyclic seven-membered ring-systems by Dieckmann-condensation avoiding usual dilution techniques and long reaction times. Thus, it significantly increases the overall yields of the pharmaceutically active ingredients azelastine and flezelastine, whose synthesis, starting from these seven-membered heterocyclic rings, is reported elsewhere. Yields range from 80-89%, avoiding waste and increasing economics of the synthesis.

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