110918-68-8

Basic information

• Product Name: (2S,3R)-3-methyl-1-tosyloxy-2-hexanol
• Synonyms: (2S,3R)-3-methyl-1-tosyloxy-2-hexanol
• CAS NO: 110918-68-8
• Molecular Weight: 286.392
• Mol File: 110918-68-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2S,3R)-3-methyl-1-tosyloxy-2-hexanol(CAS DataBase Reference)
• NIST Chemistry Reference: (2S,3R)-3-methyl-1-tosyloxy-2-hexanol(110918-68-8)
• EPA Substance Registry System: (2S,3R)-3-methyl-1-tosyloxy-2-hexanol(110918-68-8)

Safety Data

• Hazardous Substances Data: 110918-68-8(Hazardous Substances Data)

Upstream product

• 110918-65-5 (2'R,3'S)-2',3'-epoxyhexyl 3,5-dinitrobenzoate 
• 75-24-1 trimethylaluminum 
• 106498-75-3 2,3-epoxyhexanol 
• 98-59-9 p-toluenesulfonyl chloride 
• 111003-36-2 ((2R,3S)-3-propyloxiran-2-yl)methanol 
• 76741-12-3 (2S,3R)-3-methylhexane-1,2-diol 
• 76713-39-8 (2R,3R)-2-hydroxy-3-methylhexanoic acid 
• 28116-85-0 (2S,3R)-threo-2-amino-3-methylhexanoic acid 
• 60182-96-9 2-amino-3-methylhexanoic acid 
• 123-15-9 2-methylvaleraldehyde 

Downstream Products

• 110918-75-7 (2S,3S,4R)-2,4-dimethyl-3-tetrahydropyranyloxyheptyl tosylate 

Relevant articles and documents

Synthesis of (-)-Invictolide, the Pheromone Component of the Red Imported Fire Ant

(-)-Invictolide was synthesized in 16 steps from 2-methylpentanal.

Synthesis of (3S,4S)-4-Methyl-3-heptanol and Its (3S,4R)-Isomer Employing Asymmetric Epoxidation Coupled with Regioselective Cleavage of Epoxides with Trimethylaluminum

(3S,4S)-(-)-4-Methyl-3-heptanol, the key compound in the aggregation pheromone of Scolytus multistriatus Marsham, was synthesized by employing asymmetric epoxidation and epoxide cleavage with trimethylaluminum as the key steps. (3S,4R)-(+)-4-Methyl-3-heptanol was also synthesized.