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2(3H)-Furanone, 5-(1,3-dimethyl-2-cyclohexen-1-yl)dihydro-3-(1-methylethylidene)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82095-96-3

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82095-96-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82095-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,0,9 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 82095-96:
(7*8)+(6*2)+(5*0)+(4*9)+(3*5)+(2*9)+(1*6)=143
143 % 10 = 3
So 82095-96-3 is a valid CAS Registry Number.

82095-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(1,3-Dimethyl-cyclohex-2-enyl)-3-isopropylidene-dihydro-furan-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:82095-96-3 SDS

82095-96-3Downstream Products

82095-96-3Relevant academic research and scientific papers

TRANSANNULAR CYCLISATION OF ISOGERMACRONE-EPOXIDES

Tsankova, Elena,Cerrini, Silvio,Lamba, Doriano

, p. 3397 - 3404 (2007/10/02)

Isogermacrone-epoxide 2 undergoes acid- and base-induced transannular cyclisation yielding the eudesmane derivatives 8 and 12, respectively, while on treatment with Lewis acid isogermacrone-diepoxide 3 is converted into 11.The structure and stereochemistr

AN UNUSUAL REARRANGEMENT OF EUDESMANE SKELETON

Tsankova, Elena

, p. 771 - 774 (2007/10/02)

The lactone 5 was found to be a co-product of the BF3 etherate induced cyclization of epoxyisogermacrone 2.The ketol 3 when treated with 100percent HCOOH afforded the lactone 5 while under the same conditions the ketol 4 gave the corresponding ester 6.A mechanism is suggested for the rearrangements.

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