68985-16-0

Basic information

• Product Name: tosylated farnesanol
• Synonyms: tosylated farnesanol
• CAS NO: 68985-16-0
• Molecular Weight: 382.608
• Mol File: 68985-16-0.mol

Chemical Properties

• CAS DataBase Reference: tosylated farnesanol(CAS DataBase Reference)
• NIST Chemistry Reference: tosylated farnesanol(68985-16-0)
• EPA Substance Registry System: tosylated farnesanol(68985-16-0)

Safety Data

• Hazardous Substances Data: 68985-16-0(Hazardous Substances Data)

Upstream product

• 87187-93-7 (3S,7S)-3,7,11-trimethyldodecan-1-ol 
• 98-59-9 p-toluenesulfonyl chloride 
• 64610-17-9 (3S,7R)-3,7,11-trimethyldodecan-1-ol 
• 6750-34-1 3,7,11-trimethyldodecyl alcohol 

Downstream Products

• 3891-98-3 2,6,10-trimethyldodecane 
• 502-69-2 6,10,14-Trimethyl-2-pentadecanon 
• 502-69-2 (6S,10S)-6,10,14-trimethylpentadecan-2-one 

Relevant articles and documents

TYPE II CUBIC LIQUID CRYSTAL COMPOSITION

A cubic liquid crystal composition comprising at least one amphiphilic compound having the following general formula (1) and having an IV/OV value of 0.65 to 0.95, and water or an aqueous medium: wherein R represents a hydrophilic group; X and Y each inde

A New Method for the Stereochemical Analysis of Acyclic Terpenoid Carbonyl Compounds

A new method for the determination of the enantiomeric and diastereoisomeric composition of terpenoid carbonyl compounds is presented.Separation of the diastereomeric (+)-L-diisopropyl-tartrate acetals derived from dihydrocitronellal (6), hexahydropseudoionone (3), hexahydrofarnesal (7), and hexahydrofarnesylacetone (4), the C10, C13, C15, and C18 intermediates in various syntheses of naturally occuring tocopherols and vitamin K1, can be achieved by capillary GC on a cyanopropylsilicon-coated glass column under standardized conditions.This technique, presenting a significant improvment over existing methodologies, is considered to be particularly useful for the analysis of highly enriched samples, typically obtained by present-day asymmetric synthesis.With reproducibilities of +/- 0.3 percent, and therefore, safe for routine analysis, the complete stereochemical characterization of terpenoids with 15 and 18 C-atoms bearing two stereogenic centres is performed in a single operation for the first time.