96700-36-6

Basic information

• Product Name: benzoate of 13-hydroxy-(Z)-9-(E)-11-octadecadienonic acid methylester
• Synonyms: benzoate of 13-hydroxy-(Z)-9-(E)-11-octadecadienonic acid methylester
• CAS NO: 96700-36-6
• Molecular Weight: 414.585
• Mol File: 96700-36-6.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: benzoate of 13-hydroxy-(Z)-9-(E)-11-octadecadienonic acid methylester(CAS DataBase Reference)
• NIST Chemistry Reference: benzoate of 13-hydroxy-(Z)-9-(E)-11-octadecadienonic acid methylester(96700-36-6)
• EPA Substance Registry System: benzoate of 13-hydroxy-(Z)-9-(E)-11-octadecadienonic acid methylester(96700-36-6)

Safety Data

• Hazardous Substances Data: 96700-36-6(Hazardous Substances Data)

Upstream product

• 6410-93-1 methyl coriolate 
• 93-97-0 benzoic acid anhydride 
• 110623-95-5 (E)-13-benzoyloxy-1-<(tetrahydro-2H-pyran-2-yl)-oxy>-octadec-11-en-9-yn 
• 96700-33-3 (E)-13-benzoyloxy octadec-11-en-9-yn-1-al 
• 96700-30-0 (E)-13-<(tetrahydro-2H-pyran-2-yl)-oxy>-tridec-2-en-4-yn-1-al 
• 96700-34-4 Benzoic acid (E)-12-carboxy-1-pentyl-dodec-2-en-4-ynyl ester 
• 96700-32-2 (E)-13-benzoyloxy octadec-11-en-9-yn-1-ol 
• 110623-94-4 (E)-18-<(tetrahydro-2H-pyran-2-yl)-oxy>-octadec-7-en-9-yn-6-ol 
• 96700-43-5 13-<(tetrahydro-2H-pyran-2-yl)-oxy>-2,4-tridecandiyn-1-ol 
• 96700-29-7 (E)-13-<(tetrahydro-2H-pyran-2-yl)-oxy>-tridec-2-en-4-yn-1-ol 
• 17643-36-6 9-decyn-1-ol 
• 50816-19-8 8-bromooctanol 
• 629-41-4 1,8-Octanediol 
• 19754-58-6 2-dec-9-ynyloxy-tetrahydro-pyran 

Downstream Products

• 10219-69-9 (R,S)-coriolic acid 
• 10219-70-2 (13R)-hydroxylinoleic 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

A STEREOSELECTIVE SYNTHESIS OF CORIOLIC ACID AND DIMORPHECOLIC ACID

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