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2(3H)-Furanone, 3-(cyclohexylmethylene)dihydro-5-methyl-, (E)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

132209-84-8

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132209-84-8 Usage

Structure

Cyclohexylmethylene derivative of dihydro-5-methyl-2(3H)-furanone

Configuration

(E)-geometry, indicating the carbon-carbon double bond is in the E-geometry

Type of compound

Heterocyclic organic compound

Core structure

Furanone ring

Potential applications

Pharmaceutical or flavor and fragrance industries

Need for further research

To fully understand its potential uses, hazards, and toxicity

Check Digit Verification of cas no

The CAS Registry Mumber 132209-84-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,2,0 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 132209-84:
(8*1)+(7*3)+(6*2)+(5*2)+(4*0)+(3*9)+(2*8)+(1*4)=98
98 % 10 = 8
So 132209-84-8 is a valid CAS Registry Number.

132209-84-8Downstream Products

132209-84-8Relevant academic research and scientific papers

Cis-3,5-disubstituted-dihydro-furan-2-ones and the preparation and use thereof

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Page/Page column 10, (2008/06/13)

The present invention relates to an improved process to prepare cis-3-dihydrocarbylmethano-5-hydrocarbyidihydro-furan-2-ones. The present invention also relates to novel compositions of matter comprising enantiomerically pure cis-3-dihydrocarbylmethano-5-

CIS-3,5-DISUBSTITUTED-DIHYDRO-FURAN-2-ONES AND THE PREPARATION AND USE THEREOF

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Page/Page column 26, (2008/06/13)

The present invention relates to an improved process to prepare cis-3-dihydrocarbylmethano-5-hydrocarbyldihydro-furan-2-ones. The present invention also relates to novel compositions of matter comprising enantiomerically pure cis-3-dihydrocarbylmethano-5-

Spiroaziridines from 4-substituted α-ylidene-γ-butyro lactones

Gasperi, Tecla,Loreto, M. Antonietta,Migliorini, Antonella,Tardella, Paolo A.

, p. 1447 - 1454 (2007/10/03)

4-Substituted α-ylidene-γ-butyrolactones produce N-ethoxycarbonyl-spiroaziridino γ-lactone diastereomers on treatment with NsONHCO2Et and CaO. A good stereofacial preference is observed when the ring substituent is a phenyl group. These product

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