99530-30-0

Basic information

• Product Name: methyl 9-benzoyloxylinoleate
• CAS NO: 99530-30-0
• Molecular Weight: 414.585
• Mol File: 99530-30-0.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: methyl 9-benzoyloxylinoleate(CAS DataBase Reference)
• NIST Chemistry Reference: methyl 9-benzoyloxylinoleate(99530-30-0)
• EPA Substance Registry System: methyl 9-benzoyloxylinoleate(99530-30-0)

Safety Data

• Hazardous Substances Data: 99530-30-0(Hazardous Substances Data)

Upstream product

• 119238-86-7 (-)-Methyl-helenynolat 
• 119119-59-4 (E)-(S)-9-Hydroxy-11-iodo-undec-10-enoic acid methyl ester 
• 1931-63-1 methyl ester of azelaic acid aldehyde 
• 2462-84-2 methyl (9E)-octadec-9-enoate 
• 60-33-3 linoleic acid 
• 93-97-0 benzoic acid anhydride 
• 186792-27-8 9,10-epoxy-(12Z)-octadecen-1-oic acid methyl ester 
• 868364-06-1 9-10-monoepoxy-12-octadecenoic acid 
• 6084-82-8 9-hydroxy-(10E,12Z)-octadecadien-1-oic acid methyl ester 
• 98-88-4 benzoyl chloride 
• 10075-07-7 (9S,10E,12Z)-9-hydroxyoctadeca-10,12-dienoic acid methyl ester 

Downstream Products

• 10075-07-7 (9S,10E,12Z)-9-hydroxyoctadeca-10,12-dienoic acid methyl ester 

Relevant articles and documents

Preparation of the enantiomers of hydroxy-C18 fatty acids and their anti-rice blast fungus activities

In order to examine the correlation between the anti-rice blast fungus activity and the chirality of allylic alcohols 1-3, which were characterized from the infected rice plants as an enantiomeric mixture with 10% e.e., a procedure for the chemical prepa

Stereospecific Total Synthesis of Dimorphecolic Acid, 5(S)-HETE, and 12(S)-Hete

First enantiospecific synthesis of dimorphecolic acid is accomplished via an efficient and stereocontrolled route.The convenient synthesis of 5(S)-HETE and 12(S)-HETE is also described.