15734-37-9

Basic information

• Product Name: (S)-methyl abscisate
• CAS NO: 15734-37-9
• Molecular Weight: 278.348
• Mol File: 15734-37-9.mol
• Article Data: 26

Chemical Properties

• CAS DataBase Reference: (S)-methyl abscisate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-methyl abscisate(15734-37-9)
• EPA Substance Registry System: (S)-methyl abscisate(15734-37-9)

Safety Data

• Hazardous Substances Data: 15734-37-9(Hazardous Substances Data)

Upstream product

• 20109-89-1 (2Z,4E)-methyl 5-(1',4'-dihydroxy-2',6',6'-trimethyl-2'-cyclohexen-1'-yl)-3-methylpenta-2,4-dienoate 
• 2228-72-0 Abscisic acid 
• 74-88-4 methyl iodide 
• 67-56-1 methanol 
• 18107-18-1 diazomethyl-trimethyl-silane 
• 123196-50-9 (1'S,4'S)-(Z)-5-(1'-Hydroxy-2',2'-dimethyl-6'-methylene-4'-tetrahydropyranyloxycyclohexyl)-3-methyl-2-penten-5-yl tetrahydropyranyl ether 
• 123196-50-9 (1'R,4'S)-(Z)-5-(1'-Hydroxy-2',2'-dimethyl-6'-methylene-4'-tetrahydropyranyloxycyclohexyl)-3-methyl-2-penten-5-yl tetrahydropyranyl ether 
• 123196-52-1 (-)-(1'R,4'S)-(Z)-5-(1',4'-Dihydroxy-2',2'-dimethyl-6'-methylenecyclohexyl)-3-methyl-2-penten-5-yn-1-ol 
• 123196-48-5 (+)-(4R)-2,2-Dimethyl-4-tetrahydropyranyloxy-1-cyclohexanone 
• 131319-96-5 (+)-(R)-4-Hydroxy-2,2-dimethyl-1-cyclohexanone 
• 123196-49-6 (S)-6-[1-Hydroxy-meth-(Z)-ylidene]-2,2-dimethyl-4-(tetrahydro-pyran-2-yloxy)-cyclohexanone 
• 123196-53-2 (2Z,4E)-5-((1S,4S)-1,4-Dihydroxy-2,2-dimethyl-6-methylene-cyclohexyl)-3-methyl-penta-2,4-dienal 
• 123196-51-0 (+)-(1'S,4'S)-(2Z,4E)-5-(1',4'-Diydroxy-2',2'-dimethyl-6'-methylenecyclohexyl)-3-methyl-2,5-pentadien-1-ol 
• 123214-38-0 (+)-(S)-2,2-Dimethyl-6-methylene-4-tetrahydropyranyloxy-1-cyclohexanone 

Downstream Products

• 951319-47-4 methyl (1'S,2'S)-(+)-2',3'-dihydro-4'-hydroxyabscisate 
• 67-56-1 methanol 
• 2228-72-0 Abscisic acid 
• 1392295-36-1 (S,E)-methyl 3-methyl-5-(1,3,3-trimethyl-2,5-dioxocyclohexyl)pent-3-enoate 
• 1392295-37-2 (-)-(E)-methyl 4-((1S,6R,7R)-1-hydroxy-2,2,6-trimethyl-4-oxobicyclo[4.1.0]heptan-7-yl)-3-methylbut-3-enoate 

Relevant articles and documents

Synthesis and biological activity of abscisic acid esters

Abstract 16 ABA esters including 11 new compounds were prepared by two different esterification routes. All the structures of ABA esters were confirmed by 1H NMR, 13C NMR and HRMS. Their biological activity and hydrolysis stability were investigated. Fortunately, there were 15 and 9 compounds which displayed much better or nearly the same inhibition activity for rice seedling growth and Arabidopsis thaliana seed germination compared to ABA, respectively. Especially, compounds 2d and 2g showed better biological activities than ABA in the three tests. Moreover, we found that chemical hydrolysis ability of the esters in vitro had little relationship to their biological activity.

(S)-3′-methyl-abscisic acid and esters thereof

The invention relates to (S)-3′-methyl-abscisic acid, and esters thereof, and methods of using and making these compounds.

(S)-3'-METHYL-ABSCISIC ACID AND ESTERS THEREOF

The invention relates to (S)-3′-methyl-abscisic acid, and esters thereof, and methods of using and making these compounds.