134435-55-5

Basic information

• Product Name: 7-Keto-3-phenylsulfinyl-12-methoxyabieta-8,11,13-triene
• Synonyms: 7-Keto-3-phenylsulfinyl-12-methoxyabieta-8,11,13-triene
• CAS NO: 134435-55-5
• Molecular Weight: 438.631
• Mol File: 134435-55-5.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 7-Keto-3-phenylsulfinyl-12-methoxyabieta-8,11,13-triene(CAS DataBase Reference)
• NIST Chemistry Reference: 7-Keto-3-phenylsulfinyl-12-methoxyabieta-8,11,13-triene(134435-55-5)
• EPA Substance Registry System: 7-Keto-3-phenylsulfinyl-12-methoxyabieta-8,11,13-triene(134435-55-5)

Safety Data

• Hazardous Substances Data: 134435-55-5(Hazardous Substances Data)

Upstream product

• 134435-52-2 7-Cyano-3-phenylthio-12-methoxyabieta-8,11,13-triene 
• 134435-51-1 2-Geranyl-2-(3-isopropyl-4-methoxyphenyl)acetonitrile 
• 64929-62-0 3-isopropyl-4-methoxybenzyl bromide 
• 31859-25-3 4-Methoxy-3-isopropylphenylacetonitrile 
• 31825-29-3 3‐isopropyl‐4‐methoxybenzaldehyde 
• 31816-29-2 4-Methoxy-3-isopropylbenzyl alcohol 
• 24591-33-1 4-bromo-2-isopropylanisole 
• 2944-47-0 o-isopropylanisole 
• 134435-53-3 7-Oxo-3-phenylthio-12-methoxyabieta-8,11,13-triene 
• 134435-48-6 3-(1-methylethenyl)-4-methoxyphenylethyl acetate 
• 134435-50-0 (3-Isopropyl-4-methoxy-phenyl)-acetaldehyde 
• 39863-70-2 2-(3-isopropyl-4-methoxyphenyl)ethan-1-ol 
• 134435-53-3 7-Isopropyl-6-methoxy-1,1,4a-trimethyl-2-phenylsulfanyl-2,3,4,4a,10,10a-hexahydro-1H-phenanthren-9-one 
• 134435-52-2 7-cyano-3-phenylthio-12-methoxyabieta-8,11,13-triene 

Downstream Products

• 134435-54-4 7-Isopropyl-6-methoxy-1,1,4a-trimethyl-2-phenylsulfanyl-4,4a,10,10a-tetrahydro-1H-phenanthren-9-one 
• 134435-54-4 7-Keto-3-phenylthio-12-methoxyabieta-2,8,11,13-tetraene 
• 61494-73-3 3,7-Diketo-12-hydroxyabieta-8,11,13-triene 
• 61494-73-3 12-hydroxy-abieta-8,11,13-trien-3,7-dione 

Relevant articles and documents

Approach to the synthesis of candelabrone and synthesis of 3,7-diketo-12-hydroxyabieta-8,11,13-triene

An approach to the synthesis of aromatic diterpenes was tested for its generality.Phenylacetonitriles with increasing substitution on the aromatic ring were prepared and alkylated with geranyl bromide and the resulting dienes subjected to cationic cycliza