276690-18-7

Basic information

• Product Name: (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-octanoic Acid
• Synonyms: (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-octanoic Acid
• CAS NO: 276690-18-7
• Molecular Formula: C₁₉H₃₀O₅
• Molecular Weight: 324.45498
• Product Categories: Aromatics, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 276690-18-7.mol

Chemical Properties

• Boiling Point: 460.5±45.0 °C(Predicted)
• Appearance: /
• Density: 1.060±0.06 g/cm3(Predicted)
• Solubility: Dichloromethane, Ethyl Acetate
• PKA: 4.69±0.10(Predicted)
• CAS DataBase Reference: (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-octanoic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-octanoic Acid(276690-18-7)
• EPA Substance Registry System: (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-octanoic Acid(276690-18-7)

Safety Data

• Hazardous Substances Data: 276690-18-7(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-octanoic Acid is used as an intermediate in the preparation of Stigmatellin A (S686780) for its potential pharmaceutical applications. Stigmatellin A is a natural product with various biological activities, and the compound in question serves as a crucial step in its synthesis, contributing to the development of new drugs and therapies.
Used in Chemical Research:
As a complex organic molecule with specific stereochemistry, (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-octanoic Acid can be used in chemical research to study the effects of stereochemistry on the properties and reactivity of molecules. This can lead to a better understanding of molecular interactions and the development of more efficient synthetic routes for complex organic compounds.
Used in Material Science:
The compound's unique structure and properties may also find applications in material science, where it could be used to develop new materials with specific properties, such as improved stability or reactivity. Further research and development in this area could lead to innovative applications in various industries.

Upstream product

• 276690-17-6 (4S,5S,6S,7R)-(+)-1-Benzyloxy-5,7-dimethoxy-4,6-dimethyloctan-1-ol 
• 276690-12-1 (2R,3S,4S,5S)-(+)-1-Benzyloxy-2,4-dimethoxy-8-(4'-methoxyphenoxy)-3,5-dimethyloctane 

Downstream Products

• 276690-22-3 (2R,3S,4S,5S)-7-[5,7-dimethoxy-8-methoxymethoxy-3-methyl-4-oxo-4H-2-chromenyl]-2,4-dimethoxy-3,5-dimethylheptanol 
• 91682-96-1 stigmatellin A 
• 276690-20-1 (4S,5S,6S,7R)-8-Benzyloxy-5,7-dimethoxy-4,6-dimethyloctanoic acid 3,5-dimethoxy-2-methoxymethoxy-6-propionylphenyl ester 
• 276690-21-2 2-[(3S,4S,5S,6R)-7-Benzyloxy-4,6-dimethylheptyl]-5,7-dimethoxy-8-methoxymethoxy-3-methyl-4H-1-benzopyran-4-one 

Relevant articles and documents

Diastereo- and enantioselective total synthesis of stigmatellin A

Stigmatellin A (1) isolated from the myxobacterium Stigmatella aurantiaca is a powerful inhibitor of electron transport in mitochondria and chloroplasts. The first highly diastereo- and enantioselective total synthesis of this important natural product is