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63523-24-0

1-Propanone, 1,3-bis(4-methylphenyl)-3-thioxo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

63523-24-0

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63523-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 63523-24-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,5,2 and 3 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63523-24:
(7*6)+(6*3)+(5*5)+(4*2)+(3*3)+(2*2)+(1*4)=110
110 % 10 = 0
So 63523-24-0 is a valid CAS Registry Number.

63523-24-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3-bis(4-methylphenyl)-3-sulfanylidenepropan-1-one

1.2 Other means of identification

Product number -
Other names 1-Propanone,1,3-bis(4-methylphenyl)-3-thioxo

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:63523-24-0 SDS

63523-24-0Downstream Products

63523-24-0Relevant articles and documents

A novel and facile synthesis of 3,5-Disubstituted isothiozoles under metal free conditions using acetophenones and dithioesters

Nagaraju, Chaithra,Ashok, Swarup Hassan,Shamanth, Sadashivamurthy,Nagarakere, Sandhya C.,Sunilkumar, Makanahalli P.,Subbegowda, Rangappa Kanchugarakoppal,Mantelingu, Kempegowda

, p. 2647 - 2654 (2020/08/05)

A facile and conveniently simple new protocol is devised for the synthesis of 3,5-disubstituted and annulated isothiozoles under transition metal and catalyst free conditions utilizing easily available acetophenones, dithioesters and NH4OAc. This strategy involves C=O and C=S functionalization via sequential imine formation followed by intra molecular cyclization and aerial oxidation forming consecutive C?N and S?N bonds respectively in one pot. This protocol offers a low cost, user friendly, straight forward and widely applicable approach to 3,5-disubstituted isothiazoles.

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