933779-90-9

Basic information

• Product Name: (5R,6R,7RS)-5,7-bis(tert-butyldimethylsilyloxy)-6-(3-tert-butyldimethylsilyloxypropoxy)non-8-en-2-yn-1-ol
• Synonyms: (5R,6R,7RS)-5,7-bis(tert-butyldimethylsilyloxy)-6-(3-tert-butyldimethylsilyloxypropoxy)non-8-en-2-yn-1-ol
• CAS NO: 933779-90-9
• Molecular Weight: 587.076
• Mol File: 933779-90-9.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: (5R,6R,7RS)-5,7-bis(tert-butyldimethylsilyloxy)-6-(3-tert-butyldimethylsilyloxypropoxy)non-8-en-2-yn-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: (5R,6R,7RS)-5,7-bis(tert-butyldimethylsilyloxy)-6-(3-tert-butyldimethylsilyloxypropoxy)non-8-en-2-yn-1-ol(933779-90-9)
• EPA Substance Registry System: (5R,6R,7RS)-5,7-bis(tert-butyldimethylsilyloxy)-6-(3-tert-butyldimethylsilyloxypropoxy)non-8-en-2-yn-1-ol(933779-90-9)

Safety Data

• Hazardous Substances Data: 933779-90-9(Hazardous Substances Data)

Usage

Description

(5R,6R,7RS)-5,7-bis(tert-butyldimethylsilyloxy)-6-(3-tert-butyldimethylsilyloxypropoxy)non-8-en-2-yn-1-ol is a complex organic molecule with a non-8-en-2-yn-1-ol backbone and multiple functional groups, including tert-butyldimethylsilyloxy and tert-butyldimethylsilyloxypropoxy groups. These groups serve as protective or stabilizing agents in organic synthesis, enabling specific reactions to occur at other sites on the molecule. The presence of alkenes and alkynes in the structure indicates its potential involvement in organic synthesis, particularly in the formation of carbon-carbon bonds or other reactions involving unsaturated hydrocarbons. (5R,6R,7RS)-5,7-bis(tert-butyldimethylsilyloxy)-6-(3-tert-butyldimethylsilyloxypropoxy)non-8-en-2-yn-1-ol is likely used as a building block in organic chemistry for the synthesis of more complex molecules.

Uses

Used in Organic Synthesis:
(5R,6R,7RS)-5,7-bis(tert-butyldimethylsilyloxy)-6-(3-tert-butyldimethylsilyloxypropoxy)non-8-en-2-yn-1-ol is used as a building block for the synthesis of more complex organic molecules, particularly in the formation of carbon-carbon bonds or other reactions involving unsaturated hydrocarbons. The presence of protective and stabilizing groups allows for specific reactions to occur at desired sites on the molecule, making it a versatile compound in organic chemistry.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (5R,6R,7RS)-5,7-bis(tert-butyldimethylsilyloxy)-6-(3-tert-butyldimethylsilyloxypropoxy)non-8-en-2-yn-1-ol may be used as a key intermediate in the development of new drugs. Its complex structure and functional groups can be tailored to interact with specific biological targets, potentially leading to the creation of novel therapeutic agents.
Used in Chemical Research:
(5R,6R,7RS)-5,7-bis(tert-butyldimethylsilyloxy)-6-(3-tert-butyldimethylsilyloxypropoxy)non-8-en-2-yn-1-ol is also used in chemical research to study the properties and reactivity of complex organic molecules. Its unique structure and functional groups provide opportunities for investigating various reaction mechanisms and exploring new synthetic pathways in organic chemistry.
Used in Material Science:
In material science, (5R,6R,7RS)-5,7-bis(tert-butyldimethylsilyloxy)-6-(3-tert-butyldimethylsilyloxypropoxy)non-8-en-2-yn-1-ol may be employed in the development of advanced materials with specific properties. Its structural features could be utilized to create materials with tailored characteristics, such as improved stability, reactivity, or selectivity in various applications.

Downstream Products

• 200636-42-6 (Z)-2-[(3R,4R,5R)-3,5-bis(tert-butyldimethylsilyloxy)-4-(3-tert-butyldimethylsilyloxypropoxy)-2-methylenecyclohexylidene]ethanol 
• 200636-54-0 [3R-(1Z,3β,4α,5α)]-[2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-[3-[(1,1-dimethylethyl)dimethylsilyloxy]propoxy]-2-methylenecyclohexylidene]ethyl]diphenylphosphine oxide 
• 200636-50-6 [3R-(1Z,3β,4α,5α)]-2-[3,5-bis[(1,1-dimethylethyl)dimethylsilyloxy]-4-[3-[(1,1-dimethylethyl)dimethylsilyloxy]propoxy]-2-methylenecyclohexylidene]-1-chloroethane 
• 104121-92-8 Eldecalcitol