438187-09-8

Basic information

• Product Name: Benzoic acid, 2-hydroxy-6-methyl-, cyanomethyl ester
• CAS NO: 438187-09-8
• Molecular Formula: C10H9NO3
• Molecular Weight: 191.186
• Mol File: 438187-09-8.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-hydroxy-6-methyl-, cyanomethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-hydroxy-6-methyl-, cyanomethyl ester(438187-09-8)
• EPA Substance Registry System: Benzoic acid, 2-hydroxy-6-methyl-, cyanomethyl ester(438187-09-8)

Safety Data

• Hazardous Substances Data: 438187-09-8(Hazardous Substances Data)

Upstream product

• 438187-08-7 2, 2, 5-trimethyl-4H-benzo[d][1,3]dioxin-4-one 
• 164014-40-8 2,2-dimethyl-5-trifluoromethylsulfonyloxy-4H-(1,3)benzodioxin-4-one 
• 567-61-3 2-hydroxy-6-methylbenzoic acid 
• 107-14-2 chloroacetonitrile 

Downstream Products

• 438187-10-1 2-(tert-butyl-dimethyl-silanyloxy)-6-methyl-benzoic acid cyanomethyl ester 
• 438186-97-1 2-bromomethyl-6-(tert-butyl-dimethyl-silanyloxy)-benzoic acid cyanomethyl ester 
• 462629-26-1 2-[6-(tert-butyl-dimethyl-silanyloxy)-hex-2-enyl]-6-hydroxy-benzoic acid cyanomethyl ester 
• 462629-25-0 2-(tert-butyl-dimethyl-silanyloxy)-6-[6-(tert-butyl-dimethyl-silanyloxy)-hex-2-enyl]-benzoic acid cyanomethyl ester 

Relevant articles and documents

Total synthesis and stereochemical assignment of the salicylate antitumor macrolide lobatamide C

The total synthesis and stereochemical assignment of the potent antitumor macrolide lobatamide C is reported. The synthesis involves Cu(I)-mediated enamide formation and Na2CO3-mediated esterification of a β-hydroxy acid and a salicylate cyanomethyl ester. Macrolactonization was accomplished using a Mitsunobu protocol. The stereochemical assignment of lobatamide C was achieved by Mosher ester analysis and comparison with prepared stereoisomers. Copyright