107953-39-9

Upstream product

• 61668-05-1 threo-9,10,16-triacetoxyhexadecanoic acid 
• 107953-26-4 (9RS,10RS)-9,10,16-triacetoxy-1-oxo-1-(2-oxo-cyclohexyl)-hexadecane 
• 107953-31-1 (15RS,16RS)-15,16,22-trihydroxy docosanoic acid triacetate 
• 107953-32-2 1,7,8-triacetoxy-21-iodo-heneicosane 
• 107953-25-3 threo-9,10,16-triacetoxy hexadecanoyl chloride 
• 107953-27-5 (15RS,16RS)-7-oxo-15,16,22-trihydroxy docosanoic acid 
• 107953-37-7 (7RS,8RS)-7,8-isoprpylidenedioxy heneicosanal 
• 107953-29-7 (15RS,16RS)-15,16,22-trihydroxydocosanoic acid 
• 107953-36-6 (7RS,8RS)-1-hydroxy-7,8-isoprpylidenedioxy-heneicosane 
• 107953-35-5 (7RS,8RS)-1,7,8,-trihydroxy heneicosan 
• 533-87-9 threo-9,10,16-trihydroxyhexadecanoic acid 
• 107953-38-8 3-hydroxy-9,10-isopropylidenedioxytricosane 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 27519-02-4 (Z)-tricos-9-ene 
• 35857-62-6 trans-9-tricosene 

Relevant academic research and scientific papers

ENAMINE CONDENSATION ON DERIVATIVES OF ALEURITIC ACID AND SYNTHESIS OF (Z)-9-TRICOSENE (MUSCALURE), ITS (E)-ISOMER, AND (E)-13-HEPTACOSENE

Enamine condensation on (9RS,10RS)-9,10,16-triacetoxy hexadecanoyl chloride as well as (7RS,8RS)-7,8-diacetoxypentadeca-1,15-dioyl chloride using 1-morpholino-1-cyclohexene led to chain elongated products with 22 and 27 carbon atoms and its (E)-isomer while the latter led to a synthesis of (E)-13-heptacosene.