65717-26-2

Basic information

• Product Name: (5E,9E,13E,17E,21E,25E,29E,33E)-6,10,14,18,22,26,30,34,38-nonamethylnonatriaconta-5,9,13,17,21,25,29,33,37-nonaen-2-one
• Synonyms: (5E,9E,13E,17E,21E,25E,29E,33E)-6,10,14,18,22,26,30,34,38-nonamethylnonatriaconta-5,9,13,17,21,25,29,33,37-nonaen-2-one
• CAS NO: 65717-26-2
• Molecular Formula: C₄₈H₇₈O
• Molecular Weight: 671.1323
• Mol File: 65717-26-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 715°C at 760 mmHg
• Flash Point: 265.2°C
• Density: 0.884g/cm³
• Vapor Pressure: 2.72E-20mmHg at 25°C
• Refractive Index: 1.501
• CAS DataBase Reference: (5E,9E,13E,17E,21E,25E,29E,33E)-6,10,14,18,22,26,30,34,38-nonamethylnonatriaconta-5,9,13,17,21,25,29,33,37-nonaen-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5E,9E,13E,17E,21E,25E,29E,33E)-6,10,14,18,22,26,30,34,38-nonamethylnonatriaconta-5,9,13,17,21,25,29,33,37-nonaen-2-one(65717-26-2)
• EPA Substance Registry System: (5E,9E,13E,17E,21E,25E,29E,33E)-6,10,14,18,22,26,30,34,38-nonamethylnonatriaconta-5,9,13,17,21,25,29,33,37-nonaen-2-one(65717-26-2)

Safety Data

• Hazardous Substances Data: 65717-26-2(Hazardous Substances Data)

Usage

Description

(5E,9E,13E,17E,21E,25E,29E,33E)-6,10,14,18,22,26,30,34,38-nonamethylnonatriaconta-5,9,13,17,21,25,29,33,37-nonaen-2-one is a complex organic compound with a long carbon chain and multiple double bonds. It is characterized by its nonamethylnonatriaconta structure and the presence of nine double bonds in its molecular structure.

Uses

Used in Pharmaceutical Industry:
(5E,9E,13E,17E,21E,25E,29E,33E)-6,10,14,18,22,26,30,34,38-nonamethylnonatriaconta-5,9,13,17,21,25,29,33,37-nonaen-2-one is used as an intermediate in the synthesis of Isodecaprenol, a side chain of coenzyme Q10. Coenzyme Q10 is an essential component in the mitochondrial electron transport chain and plays a vital role in cellular energy production. It also has antioxidant properties and is used in the treatment of various health conditions, including heart disease, migraines, and neurodegenerative disorders.
Used in Chemical Synthesis:
(5E,9E,13E,17E,21E,25E,29E,33E)-6,10,14,18,22,26,30,34,38-nonamethylnonatriaconta-5,9,13,17,21,25,29,33,37-nonaen-2-one can be used as a building block in the synthesis of other complex organic compounds. Its unique structure with multiple double bonds and nonamethyl groups can be utilized in various chemical reactions to form new compounds with potential applications in various industries, such as pharmaceuticals, materials science, and fragrances.

Upstream product

• 80868-10-6 (5E,9E,13E,17E,21E,25E,29E,33E)-6,10,14,18,22,26,30,34,38-Nonamethyl-3-(toluene-4-sulfonyl)-nonatriaconta-5,9,13,17,21,25,29,33,37-nonaen-2-one 
• 909247-30-9 (4E,8E,12E,16E,20E,24E,28E,32E)-2-Acetyl-5,9,13,17,21,25,29,33,37-nonamethyl-octatriaconta-4,8,12,16,20,24,28,32,36-nonaenoic acid ethyl ester 
• 13190-97-1 solanesol 
• 52610-77-2 solanesyl bromide 

Downstream Products

• 15575-04-9 decaprenol 

Relevant articles and documents

IMPROVED PROCESSES FOR THE PREPARATION OF PURIFIED SOLANESOL, SOLANESYL BROMIDE AND SOLANESYL ACETONE

The present invention relates to processes for the prepartion of purified solanesol, solanesyl bromide and solanesyl acetone. Solanesyl acetone has the chemical name - all - trans 6, 10, 14, 18, 22, 26, 30, 34, 38 -nonamethyl -5,9, 13, 17, 21, 25, 29, 33, 37- triacontanonaen-2-one, of formula (I) and is used for synthesis of coenzyne Q10.

Synthesis of polyprenylacetones and -acetates; application to a new synthesis of gefarnate

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