864818-23-5

Basic information

• Product Name: (2E,8E,10E)-dodeca-2,8,10-trienal
• Synonyms: (2E,8E,10E)-dodeca-2,8,10-trienal
• CAS NO: 864818-23-5
• Molecular Weight: 178.274
• Mol File: 864818-23-5.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (2E,8E,10E)-dodeca-2,8,10-trienal(CAS DataBase Reference)
• NIST Chemistry Reference: (2E,8E,10E)-dodeca-2,8,10-trienal(864818-23-5)
• EPA Substance Registry System: (2E,8E,10E)-dodeca-2,8,10-trienal(864818-23-5)

Safety Data

• Hazardous Substances Data: 864818-23-5(Hazardous Substances Data)

Upstream product

• 110-83-8 cyclohexene 
• 55489-11-7 6,6-dimethoxyhexanal 
• 1072-21-5 hexanedial 
• 52509-14-5 (1,3-dioxolan-2-yl-methyl)triphenylphosphonium bromide 
• 95019-19-5 (2-[(N-benzylprolyl)amino]benzophenone) 
• 1530-32-1 ethyltriphenylphosphonium bromide 
• 116451-83-3 (2E,8E)-deca-2,8-diene-1,10-dial 

Downstream Products

• 935550-24-6 C₂₃H₂₉NO₄ 
• 935550-29-1 C₂₉H₄₃NO₄Si 
• 935550-28-0 C₂₃H₂₉NO₄ 
• 935550-31-5 C₂₉H₄₃NO₄Si 

Relevant articles and documents

Bidirectional, organocatalytic synthesis of lepidopteran sex pheromones

Shuffling of two simple building blocks and a regioselective transfer hydrogenation allow for the rapid synthesis of a small collection of lepidopteran sex pheromones, e.g., 8E,10Z-tetradeca-8,10-dienal 5c, from the horse chestnut leafminer (Cameraria ohridella).

Synthesis of a malimide analogue of the telomerase inhibitor UCS1025A using a dianionic aldol strategy

The synthesis of a simplified analogue of UCS1025A via an aldol coupling is described. Georg Thieme Verlag Stuttgart.