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99305-07-4

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99305-07-4 Usage

Description

(3S,4'R)-3aβ,4,5,6,6aβ,7,8,9,9aβ,9bα-Decahydro-4β-hydroxy-4'-methyl-6,9-bismethylenespiro[azuleno[4,5-b]furan-3(2H),2'-oxetan]-2-one is a complex spirocyclic lactone containing an azulene ring system and a furan ring. It has a spiro[azuleno[4,5-b]furan-3(2H),2'-oxetan]-2-one core with a decahydro-4β-hydroxy-4'-methyl-6,9-bismethylenespiro structure and a (3S,4'R)-configuration. (3S,4'R)-3aβ,4,5,6,6aβ,7,8,9,9aβ,9bα-Decahydro-4β-hydroxy-4'-methyl-6,9-bismethylenespiro[azuleno[4,5-b]furan-3(2H),2'-oxetan]-2-one is likely to have potential applications in various fields, including organic synthesis, pharmaceuticals, and materials science.

Uses

Used in Organic Synthesis:
(3S,4'R)-3aβ,4,5,6,6aβ,7,8,9,9aβ,9bα-Decahydro-4β-hydroxy-4'-methyl-6,9-bismethylenespiro[azuleno[4,5-b]furan-3(2H),2'-oxetan]-2-one is used as a key intermediate in the synthesis of complex organic molecules, particularly those containing azulene and furan ring systems. Its unique structure and stereochemistry make it a valuable building block for the development of novel compounds with potential applications in various industries.
Used in Pharmaceutical Industry:
(3S,4'R)-3aβ,4,5,6,6aβ,7,8,9,9aβ,9bα-Decahydro-4β-hydroxy-4'-methyl-6,9-bismethylenespiro[azuleno[4,5-b]furan-3(2H),2'-oxetan]-2-one is used as a potential drug candidate for the development of new therapeutic agents. Its unique structure and stereochemistry may provide novel pharmacological properties, making it a promising candidate for further research and development in the pharmaceutical industry.
Used in Materials Science:
(3S,4'R)-3aβ,4,5,6,6aβ,7,8,9,9aβ,9bα-Decahydro-4β-hydroxy-4'-methyl-6,9-bismethylenespiro[azuleno[4,5-b]furan-3(2H),2'-oxetan]-2-one is used as a component in the development of advanced materials with unique properties. Its incorporation into materials may lead to the creation of new materials with improved performance in various applications, such as sensors, catalysts, or coatings.

Check Digit Verification of cas no

The CAS Registry Mumber 99305-07-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,3,0 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 99305-07:
(7*9)+(6*9)+(5*3)+(4*0)+(3*5)+(2*0)+(1*7)=154
154 % 10 = 4
So 99305-07-4 is a valid CAS Registry Number.

99305-07-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name subexpinnatin C

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:99305-07-4 SDS

99305-07-4Downstream Products

99305-07-4Relevant articles and documents

Chemical Transformation of Deacylsubexpinnatin into the Natural Oxetane Lactone Subexpinnatin C

Collado, Isidro G.,Macias, Francisco A.,Massanet, Guillermo M.,Molinillo, Jose Maria G.,Luis, Francisco R.

, p. 3323 - 3326 (2007/10/02)

Subexpinnatin C (5), a secondary metabolite isolated from Centaurea canariensis Brouss. (var. subexpinnata Burch.), has been regio- and stereoselectively synthesized from deacylsubexpinnatin (11).This transformation involves a photoaddition reaction and a new method of obtaining the oxetane ring.

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