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158761-00-3

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158761-00-3 Usage

Description

(3S,6aS,9S,10R,10aR)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3,3a,6,6a,7,8,9,10-octahydronaphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate is a complex organic compound belonging to the class of phenolic glycosides. It features a 10-membered ring fused to a furan ring, multiple hydroxyl groups, a formyl group, and a hydroxyoctanoate side chain. This unique structure and the presence of functional groups may offer potential applications in the pharmaceutical or chemical industries.

Uses

Used in Pharmaceutical Industry:
(3S,6aS,9S,10R,10aR)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3,3a,6,6a,7,8,9,10-octahydronaphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate is used as a potential pharmaceutical agent due to its unique structure and functional groups. The presence of multiple hydroxyl and formyl groups may allow for interactions with biological targets, offering potential therapeutic benefits.
Used in Chemical Industry:
In the chemical industry, (3S,6aS,9S,10R,10aR)-4-formyl-3,10-dihydroxy-7,7-dimethyl-1-oxo-3,3a,6,6a,7,8,9,10-octahydronaphtho[1,8a-c]furan-9-yl 2-hydroxyoctanoate may be utilized as a building block or intermediate in the synthesis of other complex organic molecules. Its unique structure and functional groups can be exploited for the development of novel chemical compounds with specific properties and applications.

Check Digit Verification of cas no

The CAS Registry Mumber 158761-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,7,6 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 158761-00:
(8*1)+(7*5)+(6*8)+(5*7)+(4*6)+(3*1)+(2*0)+(1*0)=153
153 % 10 = 3
So 158761-00-3 is a valid CAS Registry Number.

158761-00-3Downstream Products

158761-00-3Relevant articles and documents

Total synthesis of mniopetals A, B, C and D

Weihrather, Joachim,Jauch, Johann

, p. 1410 - 1414 (2013/07/26)

A total synthesis of the mniopetals A, B, C and D is described. Key steps are a Sharpless asymmetric dihydroxylation and a selective esterification of an equatorial hydroxy group vicinal to an axial hydroxy function. Georg Thieme Verlag Stuttgart · New York.

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