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2(3H)-Furanone, 3-methyl-3-(4-methylphenyl)-, (S)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

141045-59-2

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141045-59-2 Usage

Chemical Family

Furanones

Stereoisomeric Form

(S)-2(3H)-Furanone, 3-methyl-3-(4-methylphenyl)-

Biological Activities

Antimicrobial, antifungal, antiviral

Odor

Fruity and sweet

Industries

Fragrance and flavor

Potential Applications

Food preservation, pest control

Check Digit Verification of cas no

The CAS Registry Mumber 141045-59-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,1,0,4 and 5 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 141045-59:
(8*1)+(7*4)+(6*1)+(5*0)+(4*4)+(3*5)+(2*5)+(1*9)=92
92 % 10 = 2
So 141045-59-2 is a valid CAS Registry Number.

141045-59-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name (S)-(-)-2-methyl-2-(4-methylphenyl)-4-but-3-enolide

1.2 Other means of identification

Product number -
Other names (S)-3-Methyl-3-p-tolyl-3H-furan-2-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:141045-59-2 SDS

141045-59-2Relevant academic research and scientific papers

Asymmetric Construction of Quaternary Carbons from Chiral Malonates: Selective and Versatile Total Syntheses of the Enantiomers of α- and β-Cuparenones from a Common Optically Active Precursor

Canet, Jean-Louis,Fadel, Antoine,Salauen, Jacques

, p. 3463 - 3473 (2007/10/02)

From a single chiron (R)-4, available with high enantiomeric purity (96percent) by simple enzymatic hydrolysis (PLE) of a prochiral malonate, were prepared convenient precursors of the two enantiomers of α- and β-cuparenones (1a,b and 2a,b).This versatile

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