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2(3H)-Furanone, dihydro-3-(4-pentenyl)-3-(phenylsulfonyl)-4-(2-propenyl)-5-propyl-, (3S,4R,5R)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

817617-05-3

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817617-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 817617-05-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,1,7,6,1 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 817617-05:
(8*8)+(7*1)+(6*7)+(5*6)+(4*1)+(3*7)+(2*0)+(1*5)=173
173 % 10 = 3
So 817617-05-3 is a valid CAS Registry Number.

817617-05-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S,4R,5R)-4-allyl-3-benzenesulfonyl-3-pentenyl-5-propyldihydrofuran-2-one

1.2 Other means of identification

Product number -
Other names (3S,4R,5R)-4-Allyl-3-benzenesulfonyl-3-pent-4-enyl-5-propyl-dihydro-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:817617-05-3 SDS

817617-05-3Downstream Products

817617-05-3Relevant academic research and scientific papers

γ-Lactones as templates in ring-closing metathesis: Enantioselective synthesis of medium sized carbocycles fused to butyrolactones

Ravelo, José Luis,Rodríguez, Carmen Ma,Martín, Víctor S.

, p. 5326 - 5335 (2007/10/03)

A methodology for accessing enantiomerically enriched carbocyclic systems fused to γ-lactones is described. Key steps are the stereoselective synthesis of highly substituted γ-lactones and ring-closing metathesis of the suitable ramifications. The process permits the choice of stereochemistry, regioselectivity and ring size of the fused compounds.

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