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6291-68-5

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6291-68-5 Usage

Molecular weight

298.21 g/mol

Type of compound

Ketone derivative

Substituent groups

Benzyl(methyl)amino group, 4-bromophenyl group

Usage

Intermediate or building block in the synthesis of pharmaceuticals and organic compounds, potential applications in medicinal chemistry and drug discovery

Handling precautions

Handle with caution, should be handled by trained professionals in a controlled laboratory setting due to potential hazardous properties.

Check Digit Verification of cas no

The CAS Registry Mumber 6291-68-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 1 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6291-68:
(6*6)+(5*2)+(4*9)+(3*1)+(2*6)+(1*8)=105
105 % 10 = 5
So 6291-68-5 is a valid CAS Registry Number.

6291-68-5SDS

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 2-[benzyl(methyl)amino]-1-(4-bromophenyl)ethanone,hydrochloride

1.2 Other means of identification

Product number -
Other names -

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:6291-68-5 SDS

6291-68-5Relevant articles and documents

Synthesis, antiulcer and antidepressive activity of 4-(4-halophenyl)-2-phenyl-1,2,3,4-tetrahydroisoquinolines

Mondeshka,Angelova,Tancheva,Ivanov,Daleva,Ivanova

, p. 475 - 480 (2007/10/02)

4-(4-halophenyl)-2-methyl-1,2,3,4-tetrahydro-isoquinolines 2a-c have been synthesized by two methods and their biochemical and pharmacological properties have been studied. Biochemical investigations showed that all the compounds are strong inhibitors of

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