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143265-98-9

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143265-98-9 Usage

Class

Benzazepine compounds

Structure

A benzene ring fused to an azepine ring

Substituents

An ethoxy group and a methyl group attached to the benzazepine ring

Appearance

White to off-white crystalline solid

Solubility

Soluble in organic solvents

Potential applications

Pharmaceutical and medicinal chemistry

Need for further research

To explore its biological activities and potential uses in the development of new drugs or therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 143265-98-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,2,6 and 5 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 143265-98:
(8*1)+(7*4)+(6*3)+(5*2)+(4*6)+(3*5)+(2*9)+(1*8)=129
129 % 10 = 9
So 143265-98-9 is a valid CAS Registry Number.

143265-98-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-ethoxy-5-methyl-1H-2-benzazepine

1.2 Other means of identification

Product number -
Other names 1H-2-Benzazepine,3-ethoxy-5-methyl

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:143265-98-9 SDS

143265-98-9Downstream Products

143265-98-9Relevant articles and documents

Base-Mediated Ring Expansion Reactions, III. A New Route from Dihydroisoquinolines to 2-Benzazepines

Groth, Ulrich,Richter, Lutz,Schoellkopf, Ulrich,Zindel, Juergen

, p. 1179 - 1184 (2007/10/02)

The substituted 2-benzazepines 4, 5, and 12 were prepared by a base-mediated ring expansion reaction of mesylates 1a-e, which where synthesized in 4 to 5 steps by starting from benzolactams 6.Key Words: 2-Benzazepines / Ring Expansion

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