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93433-64-8

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93433-64-8 Usage

Class

Substituted cathinones

Type of Compound

Stimulant and empathogenic drug

Recreational Use

Popular as a recreational substance

Structural Relation

Related to cathinone, the active ingredient in the khat plant

Effects

Increased energy, alertness, and euphoria

Psychoactive Properties

Popular among users seeking recreational use

Risks

Potential for addiction and adverse effects on physical and mental health

Legal Status

Use and distribution may be restricted or illegal in many jurisdictions

Check Digit Verification of cas no

The CAS Registry Mumber 93433-64-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,3 and 3 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 93433-64:
(7*9)+(6*3)+(5*4)+(4*3)+(3*3)+(2*6)+(1*4)=138
138 % 10 = 8
So 93433-64-8 is a valid CAS Registry Number.

93433-64-8SDS

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-methylphenyl)-2-phenylpropan-1-one

1.2 Other means of identification

Product number -
Other names 2-phenyl-1-(o-tolyl)propan-1-one

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:93433-64-8 SDS

93433-64-8Downstream Products

93433-64-8Relevant articles and documents

Pd-catalyzed Fukuyama cross-coupling of secondary organozinc reagents for the direct synthesis of unsymmetrical ketones

Cherney, Alan H.,Reisman, Sarah E.

, p. 3259 - 3265 (2014/05/06)

The coupling of acyl electrophiles with organometallic reagents represents a convergent route toward complex and versatile ketone products. Despite the mild conditions and high functional group tolerance, the cross-coupling of carboxylic acid derivatives,

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