35378-82-6

Basic information

• Product Name: 2,5,8-Undecatriyn-1-ol
• Synonyms: 2,5,8-Undecatriyn-1-ol
• CAS NO: 35378-82-6
• Molecular Formula: C₁₁H₁₂O
• Molecular Weight: 160.21238
• Mol File: 35378-82-6.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: -20°C Freezer, Under inert atmosphere
• Solubility: Dichloromethane, Ether, Ethyl Acetate, Methanol
• CAS DataBase Reference: 2,5,8-Undecatriyn-1-ol(CAS DataBase Reference)
• NIST Chemistry Reference: 2,5,8-Undecatriyn-1-ol(35378-82-6)
• EPA Substance Registry System: 2,5,8-Undecatriyn-1-ol(35378-82-6)

Safety Data

• Hazardous Substances Data: 35378-82-6(Hazardous Substances Data)

Usage

Chemical Properties

White Solid

Uses

Intermediate in the synthesis of radiolabeled fatty acids and leukotriene B5.

Synthesis Reference(s)

Tetrahedron Letters, 24, p. 4883, 1983 DOI: 10.1016/S0040-4039(01)99801-6

Upstream product

• 97526-03-9 2-undeca-2,5,8-triynyloxy-tetrahydro-pyran 
• 35378-76-8 octa-2,5-diyn-1-ol 
• 16400-32-1 1-bromo-pent-2-yne 
• 6261-22-9 pent-2-yn-1-ol 
• 1558-79-8 2,5-octadiynyl bromide 
• 34498-11-8 1-iodo-2-pentyne 
• 92666-05-2 toluene-4-sulfonic acid pent-2-ynyl ester 
• 40924-58-1 tetrahydro-2-(2,5-hexadiynyloxy)-2H-pyrane 
• 107-19-7 propargyl alcohol 

Downstream Products

• 34498-25-4 1-bromo-2,5,8-undecatriyne 
• 194721-53-4 1-tosyloxy-2,5,8-undecatriyne 
• 10417-94-4 all cis-5,8,11,14,17-eicosapentaenoic acid 
• 5871-10-3 2,5,8,11-tetradecatetrayne-1-ol 
• 194721-55-6 1-tosyloxy-2,5,8,11-tetradecatetrayne 
• 61810-56-8 (4E, 7Z, 10Z)-4,7,10-tridecatrien-1-yl acetate 
• 81309-92-4 (5Z,8Z)-cis-2,3-epoxy-5,8-undecadienyl tosylate 
• 81309-92-4 (5Z,8Z)-cis-2,3-epoxy-5,8-undecadienyl tosylate 
• 107996-57-6 (5Z,8Z)-1-(3',5'-dinitrobenzoyloxy)-cis-2,3-epoxy-5,8-undecadiene 
• 107996-57-6 (5Z,8Z)-1-(3',5'-dinitrobenzoyloxy)-cis-2,3-epoxy-5,8-undecadiene 
• 80445-66-5 (6Z,8Z,10E,14Z,17Z)-(5S,12R)-5,12-Dihydroxy-icosa-6,8,10,14,17-pentaenoic acid 
• 2566-90-7 all-cis-4,7,10,13,16,19-docosahexaenoic acid methyl ester 
• 5871-06-7 1-bromotetradeca-2,5,8,11-tetrayne 
• 24880-40-8 eicosatetraenoic acid 

Relevant articles and documents

Synthesis of Rare Polyunsaturated Fatty Acids: Stearidonic and ω-3 Arachidonic

Total chemical syntheses of the rare natural ω-3 C18 and C20 fatty acids, which possess potential antiinflammatory activity, were elaborated for subsequent studies of their biological activity.

METHOD FOR THE SYNTHESIS OF DHA

A method for preparing docosahexaenoic acid (DHA). The method comprises coupling a compound represented by Formula I with a compound represented by Formula II followed by partial hydrogenation to obtain a compound represented by Formula III. The compound represented by Formula III acts as a DHA precursor and thus can be hydrolysed to obtain DHA. Novel starting materials represented by Formula I and Formula II, and synthetic routes for preparing the same are also provided.

SYNTHESES OF OPTICALLY ACTIVE PHEROMONES WITH AN EPOXY RING, (+)-DISPARLURE AND BOTH THE ENANTIOMERS OF (3Z,6Z)-cis-9,10-EPOXY-3,6-HENEICOSADIENE

(+)-Disparlure 1 and both the enantiomers of (3Z,6Z)-cis-9,10-epoxy-3,6-heneicosadiene 2 were synthesized in optically pure forms employing the Sharpless asymmetric epoxidation as the key-step.The natural pheromone 2 isolated from Estigmene acrea was shown to possess (9S,10R)-stereochemistry.