78907-89-8

Basic information

• Product Name: 1,4-Dithiaspiro[4.4]non-6-ene-6-carboxaldehyde, 8-(phenylmethoxy)-, (R)-
• CAS NO: 78907-89-8
• Molecular Formula: C15H16O2S2
• Molecular Weight: 292.423
• Mol File: 78907-89-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 1,4-Dithiaspiro[4.4]non-6-ene-6-carboxaldehyde, 8-(phenylmethoxy)-, (R)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,4-Dithiaspiro[4.4]non-6-ene-6-carboxaldehyde, 8-(phenylmethoxy)-, (R)-(78907-89-8)
• EPA Substance Registry System: 1,4-Dithiaspiro[4.4]non-6-ene-6-carboxaldehyde, 8-(phenylmethoxy)-, (R)-(78907-89-8)

Safety Data

• Hazardous Substances Data: 78907-89-8(Hazardous Substances Data)

Upstream product

• 78907-87-6 (3R,4S,5R)-5-O-benzyl-3,4,5-trihydroxycyclohexanone ethylene dithioacetal 
• 77003-65-7 (3R,4S,5R)-3,4,5-trihydroxycyclohexanone ethylene dithioacetal 
• 78907-88-7 (2R)-2-benzyloxy-4-oxo-1,6-hexanedial 4-ethylene dithioacetal 

Downstream Products

• 82302-57-6 11α-hydroxy-13-oxaprostanoic acid 
• 78907-91-2 (3R)-benzyloxy-5-oxo-1-cyclopentene-1-carbaldehyde 1-propylene acetal 
• 78907-94-5 (1R,2R,3S)-benzyloxy-3-hydroxy-2-cyclopentanecarbaldehyde trimethylene-acetal 
• 78963-78-7 (1R,2S,3S)-benzyloxy-3-hydroxy-2-cyclopentanecarbaldehyde trimethylene-acetal 
• 78907-93-4 (1S,2R,3R)-benzyloxy-3-heptyloxy-2-(oxo-5-ethylene-dithioacetal)cyclopentanecarbaldehyde trimethylene-acetal 
• 78907-95-6 1α-benzyloxy-3α-(1,3-dioxa-2-cyclohexyl)-2β-heptyloxycyclopentane 
• 78907-92-3 (1S,2R,3R)-benzyloxy-3-hydroxy-2-(oxo-5-ethylene-dithioacetal)cyclopentanecarbaldehyde trimethylene-acetal 
• 78907-98-9 (1S,2R,3R)-benzyloxy-3-heptyloxy-2-cyclopentanecarbaldehyde 
• 78907-97-8 (1R,2R,3S)-benzyloxy-3-oxo-2-cyclopentanecarbaldehyde trimethylene-acetal 
• 78907-90-1 (3R)-3-benzyloxy-5-oxo-1-cyclopentene-1-carbaldehyde 1-propylene-acetal 5-ethylene-dithioacetal 

Relevant articles and documents

Hetero-prostaglandin derivatives and processes for preparing them

Prostanoic acid derivatives represented by the general formula: STR1 in which X represents hydrogen or hydroxy, X1 represents hydrogen or X and X1, when they are taken together with the carbon atom to which they are attached, represent a carbonyl group and Z represents hydrogen or hydroxy and pharmaceutically acceptable alkali metal salts thereof. They can be used as bronchodilators and/or inhibitors of blood-platelet aggregation.

Synthesis of reactive intermediates for natural cyclopentane derivatives from (-)-quinic acid: Preparation of 11α-hydroxy-13-oxaprostanoic acid

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