276690-17-6

Basic information

• Product Name: (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-1-octanol
• Synonyms: (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-1-octanol
• CAS NO: 276690-17-6
• Molecular Formula: C₁₉H₃₂O₄
• Molecular Weight: 103.16282
• Product Categories: Aromatics, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 276690-17-6.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 421.8±45.0 °C(Predicted)
• Appearance: /
• Density: 1.007±0.06 g/cm3(Predicted)
• Solubility: Dichloromethane, Ethyl Acetate
• PKA: 15.13±0.10(Predicted)
• CAS DataBase Reference: (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-1-octanol(CAS DataBase Reference)
• NIST Chemistry Reference: (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-1-octanol(276690-17-6)
• EPA Substance Registry System: (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-1-octanol(276690-17-6)

Safety Data

• Hazardous Substances Data: 276690-17-6(Hazardous Substances Data)

Usage

Description

(4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-1-octanol is a complex organic compound characterized by its molecular structure and chemical properties. It is a colorless oil, indicating that it is a liquid at room temperature and has a relatively low molecular weight. (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-1-octanol is an intermediate in the preparation of Stigmatellin A (S686780), which suggests its importance in the synthesis of biologically active molecules.

Uses

1. Used in Pharmaceutical Industry:
(4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-1-octanol is used as an intermediate in the synthesis of Stigmatellin A (S686780) for its potential pharmaceutical applications. Stigmatellin A is a natural product with known biological activities, and this compound plays a crucial role in its production process.
2. Used in Chemical Research:
As a complex organic molecule, (4S,5S,6S,7R)-5,7-DiMethoxy-4,6-diMethyl-8-(phenylMethoxy)-1-octanol can be used in chemical research to study its properties, reactivity, and potential applications in various chemical reactions. Its unique structure may offer insights into the development of new synthetic routes and the creation of novel compounds with specific functionalities.
3. Used in Material Science:
The compound's properties as a colorless oil may make it suitable for use in material science, where it could be explored for potential applications in the development of new materials with specific characteristics, such as improved solubility, stability, or reactivity.

Upstream product

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

Downstream Products

• 276690-18-7 (4S,5S,6S,7R)-(+)-1-Benzyloxy-5,7-dimethoxy-4,6-dimethyloctanoic acid 
• 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