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57930-46-8

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  • (3aR,4S,5R,6aS)-4-[(Acetyloxy)methyl]hexahydro-5-hydroxy-2H-cyclopenta[b]furan-2-one

    Cas No: 57930-46-8

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57930-46-8 Usage

General Description

The chemical compound "(3aR,4S,5R,6aS)-4-[(Acetyloxy)methyl]hexahydro-5-hydroxy-2H-cyclopenta[b]furan-2-one" is a complex organic molecule with a cyclopentane ring structure. It contains an acetyloxy group and a hydroxy group, giving it both ester and alcohol functionalities. The compound has a six-membered ring with a lactone structure, and the acetyloxy group is attached to the fourth position of the ring. (3aR,4S,5R,6aS)-4-[(Acetyloxy)methyl]hexahydro-5-hydroxy-2H-cyclopenta[b]furan-2-one may have potential pharmaceutical or biological activities due to its unique structure and functional groups.

Check Digit Verification of cas no

The CAS Registry Mumber 57930-46-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,7,9,3 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 57930-46:
(7*5)+(6*7)+(5*9)+(4*3)+(3*0)+(2*4)+(1*6)=148
148 % 10 = 8
So 57930-46-8 is a valid CAS Registry Number.

57930-46-8SDS

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 [(3aR,4S,5R,6aS)-5-Hydroxy-2-oxohexahydro-2H-cyclopenta[b]furan-4 -yl]methyl acetate

1.2 Other means of identification

Product number -
Other names (1S,5R)-(+)-nopinone

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:57930-46-8 SDS

57930-46-8Relevant articles and documents

Prins Reaction of 2-Oxabicyclooct-6-en-3-one and Related Derivatives

Toemoeskoezi, Istvan,Gruber, Lajos,Baitz-Gacs, Eszter

, p. 10345 - 10352 (2007/10/02)

Reaction of formaldehyde with the title olefinic lactone in acetic acid affords diacetate of 1,3-diol (2a) as the main product in 50-60percent yield via regioselective trans-addition.Less favourable results were obtained with related bicyclic derivatives.

Efficient enzymatic preparation of (+)- and (-)Corey lactone derivatives

Sugahara,Satoh,Yamada,Takano

, p. 2758 - 2760 (2007/10/02)

Two pairs of Corey lactone derivatives, (+)-1, (-)-2 and (+)-3, (-)-4 have been efficiently prepared in high optical purity by enzymatic esterification and enzymatic hydrolysis catalyzed by lipases from Pseudomonas sp.

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