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2-(1,3-dithiolan-2-ylidene)-1-phenyl-1,3-butanedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

74440-20-3

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74440-20-3 Usage

Structure

Contains a dithiolane ring and a phenyl group attached to a butanedione moiety

Classification

Organic compound

Usage

Commonly used as a reagent in organic synthesis, particularly in the preparation of heterocyclic compounds and pharmaceuticals

Radical scavenging properties

Potential to act as a radical scavenger, making it useful in the study of oxidative stress and free radical biology

Biological and pharmacological applications

Has shown potential in various biological and pharmacological applications due to its unique structure and reactivity

Check Digit Verification of cas no

The CAS Registry Mumber 74440-20-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,4 and 0 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 74440-20:
(7*7)+(6*4)+(5*4)+(4*4)+(3*0)+(2*2)+(1*0)=113
113 % 10 = 3
So 74440-20-3 is a valid CAS Registry Number.
InChI:InChI=1/C13H12O2S2/c1-9(14)11(13-16-7-8-17-13)12(15)10-5-3-2-4-6-10/h2-6H,7-8H2,1H3

74440-20-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1,3-dithiolan-2-ylidene)-1-phenylbutane-1,3-dione

1.2 Other means of identification

Product number -
Other names KZ 1026

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:74440-20-3 SDS

74440-20-3Relevant academic research and scientific papers

A clean, facile, and stereospecific synthesis of α-oxoketene O,S-acetals in water

Li, Yan,Zhang, Qian,Cheng, Xin,Liu, Qun,Xu, Xiaohong

experimental part, p. 824 - 828 (2009/07/25)

A facile and practical method for the stereospecific synthesis of α-oxoketene O,S-acetals in water has been developed. Catalyzed by tetrabutylammonium bromide at room temperature, the one-pot reaction of various β-dicarbonyl compounds, 2-bromoethanol, and

Studies on the one-pot reaction of active methylene compounds with 2-bromoethanol - Preparation of α-oxoketene cyclic O,S-ethylene acetals

Shu-Jia,Qun,Yao-Zu

, p. 147 - 150 (2007/10/03)

Active methylene compounds 3 react with CS2, 2-bromoethanol in the presence of K2CO3 to give two products 4 and 5 through one-pot reaction. Acylketene cyclic O.S-ethylene acetals 10 have been synthesized by the displacemen

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