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(1aS,7R,7aR,10aS,11aS)-1a,2,3,7a,8,10a,11,11a-Octahydro-11a-methyl-8-methylene-5H-7,4-methenofuro[3,2-c]oxireno[f]oxacycloundecin-5,9(7H)-dione is a complex organic compound characterized by a unique fused ring structure. It is composed of 12 carbon atoms and features multiple functional groups, including a ketone and an epoxide, which contribute to its high unsaturation. The presence of the epoxide ring endows the molecule with potential reactivity, suggesting possible biological activity or applications in organic synthesis. The intricate structure and diverse functional groups make (1aS,7R,7aR,10aS,11aS)-1a,2,3,7a,8,10a,11,11a-Octahydro-11a-methyl-8-methylene-5H-7,4-methenofuro[3,2-c]oxireno[f]oxacycloundecin-5,9(7H)-dione a promising subject for further research in chemistry and pharmacology.

23753-57-3

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23753-57-3 Usage

Uses

Used in Organic Synthesis:
(1aS,7R,7aR,10aS,11aS)-1a,2,3,7a,8,10a,11,11a-Octahydro-11a-methyl-8-methylene-5H-7,4-methenofuro[3,2-c]oxireno[f]oxacycloundecin-5,9(7H)-dione is used as a key intermediate in organic synthesis for the preparation of various complex organic molecules. Its unique structure and functional groups provide opportunities for further chemical modifications and the development of novel compounds with potential applications in various fields.
Used in Pharmaceutical Research:
In the pharmaceutical industry, (1aS,7R,7aR,10aS,11aS)-1a,2,3,7a,8,10a,11,11a-Octahydro-11a-methyl-8-methylene-5H-7,4-methenofuro[3,2-c]oxireno[f]oxacycloundecin-5,9(7H)-dione is used as a starting material for the development of new drugs. Its potential reactivity and the presence of multiple functional groups make it an attractive candidate for the design of bioactive molecules with therapeutic properties. Further research is needed to explore its potential as a lead compound in drug discovery programs.
Used in Chemical Research:
(1aS,7R,7aR,10aS,11aS)-1a,2,3,7a,8,10a,11,11a-Octahydro-11a-methyl-8-methylene-5H-7,4-methenofuro[3,2-c]oxireno[f]oxacycloundecin-5,9(7H)-dione serves as a valuable subject for chemical research, particularly in the study of reaction mechanisms and the development of new synthetic methods. Its complex structure and the presence of the epoxide ring offer opportunities to investigate its reactivity and explore novel transformations, contributing to the advancement of organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 23753-57-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,7,5 and 3 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 23753-57:
(7*2)+(6*3)+(5*7)+(4*5)+(3*3)+(2*5)+(1*7)=113
113 % 10 = 3
So 23753-57-3 is a valid CAS Registry Number.

23753-57-3SDS

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 Deoxymihanolid

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:23753-57-3 SDS

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