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79831-77-9

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79831-77-9 Usage

Chemical class

Indolizine derivatives
This compound belongs to a group of chemical compounds derived from indolizine, a tricyclic aromatic organic compound.

Octahydro derivative

The compound is an octahydro derivative of indolizine, meaning it has eight hydrogen atoms added to the indolizine structure.

Tetraacetate (ester)

The compound has four acetate groups attached to it, making it a tetraacetate ester.

Stereochemistry

1S, 6S, 7R, 8R, and 8aR configuration
The compound has a specific arrangement of its chiral centers, which is important for its potential applications and interactions with other molecules.

Chiral centers

Five chiral centers
The compound has five chiral centers, which contribute to its stereochemistry and potential biological activity.

Potential applications

Pharmaceutical industry or synthesis of other compounds
The compound may have potential uses in the pharmaceutical industry or as a building block for the synthesis of other compounds.

Further research

Properties and uses to be determined
The specific properties and potential uses of this compound may be determined through further research and investigation.

Molecular structure

Tricyclic aromatic compound with ester functional groups
The compound has a complex molecular structure, featuring a tricyclic aromatic core and ester functional groups attached to it.

Solubility

Unknown, may depend on the solvent and concentration
The solubility of this compound is not provided, but it may vary depending on the solvent and concentration used.

Stability

Unknown, may require specific conditions for stability
The stability of this compound is not provided, but it may require specific conditions (e.g., temperature, pH, or solvent) to maintain its structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 79831-77-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,8,3 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 79831-77:
(7*7)+(6*9)+(5*8)+(4*3)+(3*1)+(2*7)+(1*7)=179
179 % 10 = 9
So 79831-77-9 is a valid CAS Registry Number.

79831-77-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,6,7,8-tetra-O-acetylcastanospermine

1.2 Other means of identification

Product number -
Other names castanospermine tetraacetate

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:79831-77-9 SDS

79831-77-9Relevant articles and documents

Novel synthesis of castanospermine and 1-epicastanospermine

Cronin, Linda,Murphy, Paul V.

, p. 2691 - 2693 (2007/10/03)

(Chemical Equation Presented) Polyhydroxylated indolizidines have potential for treatment of HIV, hepatitis C and HSV infection, multiple sclerosis, angiogenesis, cancer, and diabetes. A new synthetic approach to the title compounds from a 5-C-methoxypyra

A concise, enantioselective synthesis of castanospermine

Kim,Choi,Cha

, p. 7096 - 7099 (2007/10/02)

A stereoselective synthesis of the polyhydroxy indolizidine alkaloids castanospermine (1) and 6,7-diepicastanospermine (4) has been achieved starting from the readily available alcohol 8. Subsequent Sharpless asymmetric epoxidation, followed by the azide displacement of the tosyl group gave the epoxy azide 12. The asymmetric dihydroxylation of 12 with (DHQ)2-PHAL gave tbe triol 13 in good diastereoselectivity. Alcohol protection, followed by reductive double cyclization of the resulting epoxy azide 17 gave 5-indolizidinone 18, which was then uneventfully converted to 1. On the other hand, the use of (DHQD)2-PHAL in the dihydroxylation of 12 provided a stereoselective preparation of 4.

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