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(1S,6S,7S,8R,8aR)-1,7,8-trihydroxyoctahydroindolizin-6-yl furan-2-carboxylate is a complex chiral chemical compound characterized by a central indolizine ring with three hydroxyl groups and a furan-2-carboxylate moiety attached. Its unique molecular structure, featuring multiple asymmetric carbon centers, may confer potential pharmacological and biological activities, making it a candidate for further research in diverse fields such as medicine, agriculture, and materials science.

121104-92-5

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121104-92-5 Usage

Uses

Used in Pharmaceutical Industry:
(1S,6S,7S,8R,8aR)-1,7,8-trihydroxyoctahydroindolizin-6-yl furan-2-carboxylate is used as a potential pharmaceutical agent for its possible biological activities. Given its unique structure, it may be developed into a drug candidate for treating various medical conditions once its specific properties and mechanisms of action are elucidated through further research.
Used in Agricultural Applications:
In agriculture, (1S,6S,7S,8R,8aR)-1,7,8-trihydroxyoctahydroindolizin-6-yl furan-2-carboxylate could be utilized as a bioactive compound for pest control or as a component in the development of new plant protection products. Its potential use in this industry would depend on the results of research into its effects on pests and plants, as well as its environmental safety.
Used in Materials Science:
(1S,6S,7S,8R,8aR)-1,7,8-trihydroxyoctahydroindolizin-6-yl furan-2-carboxylate may also find applications in materials science, potentially serving as a component in the development of new materials with specific properties. Its unique molecular structure could contribute to the creation of innovative materials with applications in various industries, pending further exploration into its material properties and compatibility.

Check Digit Verification of cas no

The CAS Registry Mumber 121104-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,1,0 and 4 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 121104-92:
(8*1)+(7*2)+(6*1)+(5*1)+(4*0)+(3*4)+(2*9)+(1*2)=65
65 % 10 = 5
So 121104-92-5 is a valid CAS Registry Number.

121104-92-5SDS

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 [(1S,6S,7S,8R,8aR)-1,7,8-trihydroxy-1,2,3,5,6,7,8,8a-octahydroindolizin-6-yl] furan-2-carboxylate

1.2 Other means of identification

Product number -
Other names 6-O-(2-Furoyl)tanospermine

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:121104-92-5 SDS

121104-92-5Upstream product

121104-92-5Downstream Products

121104-92-5Relevant articles and documents

Combinations of retroviral inhibitors

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, (2008/06/13)

The combination of compounds of formula I and II can be used for the treatment of retroviraI infections. The combination can be used to treat AIDS and ARC and other diseases caused by the retrovirus HTV or other related viruses.

Esters of castanospermine in the treatment of cerebral malaria

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, (2008/06/13)

Red blood cells which are infected with the parasite P. falciparum cause the cells to become sticky and less deformable. This results in a build-up of cells on the vascular wall and creates occlusions to blood flow which are thought to cause the cerebral, renal and liver complications of P. falciparum infections. Certain esters of castanospermine prevent or reduce the adhesion of falciparum infected blood cells to the vascular endothelial wall and are a useful adjunct in the treatment of malaria.

Castanospermine esters and glycosides

-

, (2008/06/13)

Castanospermine mono- and di-esters and glycosides active as inhibitors of carbohydrate digestive enzymes and useful in treating diabetes are described herein. The compounds are prepared by the reaction of castanospermine with an appropriate acid halide or anhydride or with an appropriate glycosyl halide or glycosyl acetimidate under conditions which would favor the isolation of the mono- and di-esterified and glycosylated products. Various blocking groups, which can be selectively removed under mild conditions, can also be used to favor the formation of certain isomers.

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