141339-58-4

Basic information

• Product Name: Benzoic acid, 4-methyl-, 2-oxoheptyl ester
• CAS NO: 141339-58-4
• Molecular Formula: C15H20O3
• Molecular Weight: 248.322
• Mol File: 141339-58-4.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 4-methyl-, 2-oxoheptyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 4-methyl-, 2-oxoheptyl ester(141339-58-4)
• EPA Substance Registry System: Benzoic acid, 4-methyl-, 2-oxoheptyl ester(141339-58-4)

Safety Data

• Hazardous Substances Data: 141339-58-4(Hazardous Substances Data)

Upstream product

• 41055-92-9 1-chloro-2-heptanone 
• 16518-25-5 potassium p-methyl benzoate 
• 141339-93-7 t-butyl 2-chloro-3-oxooctanoate 
• 66720-07-8 tert-butyl 3-oxooctanoate 

Relevant articles and documents

A Systematic Study on the Bakers'Yeast Reduction of 2-Oxoalkyl Benzoates and 1-Chloro-2-alkanones

The bakers' yeast reduction of a series of 2-oxoalkyl arenecarboxylates (1a-f) (R=CH3 to n-C6H13; X=H) and the phenyl-modified derivatives (1g-l) (R=n-C5H11, X=OH, CH3, F, Cl, Br, or I) as well as 1-chloro-2-alkanones R(C=O)CH2Cl (6a-f) (R=CH3 to n-C6H13) were systematically investigated.The substrate specificities, configuration and percentee of the reduction products were found to be highly dependent on the length of the alkyl group (R) and the α substituent.Thus, the benzoates 1a-f gave optically active 2-hydroxyalkyl benzoates (2a-f) (R, configuration, percentee) (a: CH3, S, 99; b: C2H5, S, 98; c: C3H7, S, 26; d: n-C4H9, R, 55; e: n-C5H11, S, 15; f: n-C6H13, S, 63) in 11-91percent yields.Among the modification experiments of the phenyl group, 1g-l, the p-iodo substituent markedly increased the ee from 15 to 71percent, although the yield was rather lowered (22percent yield).The reduction of α-chloro ketones 6a-f also gave optically active 1-chloro-2-alkanols (7a-f) in 16-69percent yields.