133744-43-1

Basic information

• Product Name: (S)-p-Mentha-1,8-dien-7-yl benzoate
• CAS NO: 133744-43-1
• Molecular Weight: 256.345
• Mol File: 133744-43-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-p-Mentha-1,8-dien-7-yl benzoate(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-p-Mentha-1,8-dien-7-yl benzoate(133744-43-1)
• EPA Substance Registry System: (S)-p-Mentha-1,8-dien-7-yl benzoate(133744-43-1)

Safety Data

• Hazardous Substances Data: 133744-43-1(Hazardous Substances Data)

Upstream product

• 100-52-7 benzaldehyde 
• 536-59-4 (-)-perillyl alcohol 
• 98-88-4 benzoyl chloride 

Downstream Products

• 133744-44-2 (S)-8-Hydroxy-p-menth-1-en-7-yl benzoate 
• 133744-46-4 (S)-8-Amino-p-menth-1-en-7-yl benzoate 
• 133744-45-3 Benzoic acid (S)-4-(1-azido-1-methyl-ethyl)-cyclohex-1-enylmethyl ester 
• 145801-24-7 (1R,4R,5S,7R)-4-[1-(4-Methoxy-benzenesulfonyl)-1H-indol-3-ylmethyl]-2,2-dimethyl-6-methylene-3-aza-tricyclo[3.3.1.0^3,7]nonane 
• 133744-50-0 1-[(4-methoxyphenyl)sulfonyl]hobartine 
• 133744-49-7 (+)-1-<(4-Methoxyphenyl)sulfonyl>-20-(phenylthio)hobartine 
• 133744-47-5 (R)-8-Amino-p-menth-1-en-7-ol 
• 133744-47-5 (S)-8-Amino-p-menth-1-en-7-ol 
• 133744-48-6 (R)-7-(Phenylthio)-p-menth-1-en-8-amine 
• 133744-48-6 (S)-7-(Phenylthio)-p-menth-1-en-8-amine 

Relevant articles and documents

Photochemical Activation of Aromatic Aldehydes: Synthesis of Amides, Hydroxamic Acids and Esters

A cheap, facile and metal-free photochemical protocol for the activation of aromatic aldehydes has been developed. Utilizing thioxanthen-9-one as the photocatalyst and cheap household lamps as the light source, a variety of aromatic aldehydes have been activated and subsequently converted in a one-pot reaction into amides, hydroxamic acids and esters in good to high yields. The applicability of this method was highlighted in the synthesis of Moclobemide, a drug against depression and social anxiety. Extended and detailed mechanistic studies have been conducted, in order to determine a plausible mechanism for the reaction.