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1-Propanone, 2-(methylsulfonyl)-1,3-diphenyl-, also known as 1,3-Diphenyl-2-(methylsulfonyl)propan-1-one, is an organic compound with the chemical formula C16H16O3S. It is a colorless to pale yellow crystalline solid with a molecular weight of 292.36 g/mol. 1-Propanone, 2-(methylsulfonyl)-1,3-diphenyl- is characterized by the presence of a propanone (acetone) backbone, with two phenyl groups attached to the first and third carbon atoms, and a methylsulfonyl group attached to the second carbon atom. It is used as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, particularly in the production of certain pesticides and drugs. Due to its reactivity and potential applications, it is important to handle 1-Propanone, 2-(methylsulfonyl)-1,3-diphenyl- with care, following proper safety protocols.

3708-06-3

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3708-06-3 Usage

Chemical class

Cathinone (synthetic stimulant drug)

Structural relation

MDPV (similar properties as a psychoactive substance)

Effects

Stimulant (increased energy, alertness, empathy)

Side effects and risks

Potential addiction, cardiovascular issues, psychiatric disturbances

Legal status

Schedule I controlled substance in the United States, legal restrictions in many other countries.

Check Digit Verification of cas no

The CAS Registry Mumber 3708-06-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,0 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3708-06:
(6*3)+(5*7)+(4*0)+(3*8)+(2*0)+(1*6)=83
83 % 10 = 3
So 3708-06-3 is a valid CAS Registry Number.

3708-06-3SDS

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 α-benzyl-β-keto sulfone

1.2 Other means of identification

Product number -
Other names 2-methanesulfonyl-1,3-diphenyl-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:3708-06-3 SDS

3708-06-3Relevant academic research and scientific papers

Synthesis of arylethyl (E)-styrylsulfones and arylsulfones by one-pot DIBAL-H/NaH-mediated reaction of β-ketosulfones

Chang, Meng-Yang,Chen, Yi-Chia,Chan, Chieh-Kai

, p. 1739 - 1744 (2014/08/05)

A facile one-pot synthetic route for preparing a series of arylethyl (E)-styrylsulfones or arylethyl arylsulfones is developed. The efficient one-pot DIBAL-H/NaH-mediated route includes reduction of α-benzyl-β- arylketosulfones and retroaldol/aldol or retro aldol reaction of the resulting intermediate. The DIBAL-H/NaH-mediated reaction mechanism has been discussed. Georg Thieme Verlag Stuttgart. New York.

TANDEM REDUCTION-DESULFONYLATION OF α-ALKYLIDENE-β-KETO SULFONES

Huang, Xian,Zhang, Han-zhong

, p. 97 - 106 (2007/10/02)

α-Alkylidene-β-keto sulfones take place both reduction of carbon-carbon double bond and desulfonylation with the use of sodium hydrogen telluride in ethanol-N,N-dimethylformamide.

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