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4412-04-8

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4412-04-8 Usage

Structure

A derivative of benzofuranone with a 3-ethylidene group

Usage

Production of fragrances and flavorings due to its pleasant and sweet odor

Potential applications

Pharmaceutical industry as a building block for the synthesis of various bioactive compounds

Stability

Stable and non-reactive nature, making it useful for a wide range of industrial and commercial applications

Antimicrobial properties

Has been studied for its potential antimicrobial properties

Anticancer properties

Has been studied for its potential anticancer properties

Check Digit Verification of cas no

The CAS Registry Mumber 4412-04-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,4,1 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4412-04:
(6*4)+(5*4)+(4*1)+(3*2)+(2*0)+(1*4)=58
58 % 10 = 8
So 4412-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H8O2/c1-2-7-8-5-3-4-6-9(8)12-10(7)11/h2-6H,1H3/b7-2+

4412-04-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name (3E)-3-ethylidene-1-benzofuran-2-one

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:4412-04-8 SDS

4412-04-8Downstream Products

4412-04-8Relevant articles and documents

Designing a catalytic synthesis of 4-methylcoumarin from ortho-iodophenyl 3-butenoate: Ring closure and isomerization control

Catellani, Marta,Chiusoli, Gian Paolo,Marzolini, Giovanna,Rossi, Emanuela

, p. 65 - 69 (2007/10/03)

The palladium-catalyzed ring closure of ortho-iodophenyl 3-butenoate to 4-methylcoumarin is in competition with the isomerization to the 2-butenoic ester; the latter reaction has been controlled by the appropriate use of ligands, solvents and neutralizing agents to the point that quantitative yields of the cyclic compound have been attained.

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