70894-19-8

Basic information

• Product Name: oxalic acid monomenthyl ester
• Synonyms: oxalic acid monomenthyl ester
• CAS NO: 70894-19-8
• Molecular Weight: 228.288
• Mol File: 70894-19-8.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: oxalic acid monomenthyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: oxalic acid monomenthyl ester(70894-19-8)
• EPA Substance Registry System: oxalic acid monomenthyl ester(70894-19-8)

Safety Data

• Hazardous Substances Data: 70894-19-8(Hazardous Substances Data)

Upstream product

• 2216-51-5 (-)-menthol 
• 144-62-7 oxalic acid 
• 117530-32-2 methyl-((1R)-menthyl)-oxalate 
• 79-37-8 oxalyl dichloride 

Downstream Products

• 500-00-5 3-p-menthene 
• 2085-26-9 bis[(1R,2S,5R)-2-isopropyl-5-methylcyclohexyl]oxalate 
• 154002-63-8 2-((1R,5R)-2-isopropyl-5-methylcyclohexyl)-4-methylquinoline 
• 16052-42-9 (1R,2S,5R)-menthyl chloride 
• 13371-12-5 neomenthyl chloride 
• 2085-26-9 ((1R)-menthyl)-((1S)-menthyl)-oxalate 
• 81529-62-6 (1R,2S,5R)-2-isopropyl-5-methylcyclohexyl 2-chloro-2-oxoacetate 

Relevant articles and documents

Metal-, Photocatalyst-, and Light-Free Minisci C-H Alkylation of N-Heteroarenes with Oxalates

Herein, we report a mild protocol for metal-, photocatalyst-, and light-free Minisci C-H alkylation reactions of N-heteroarenes with alkyl oxalates derived from primary, secondary, and tertiary alcohols. The protocol uses environmentally benign persulfate

Reductive Addition to Electron-deficient Olefins with Trivalent Iodine Compounds

(Diacyloxyiodo)arene was treated with electron-deficient olefins in the presence of hydrogen donor such as 1,4-cyclohexadiene to give the reductive addition products via alkyl radical through the radical decarboxylative pathway in good yields.Moreover, this system was able to generate either alkoxycarbonyl radicals or alkyl radicals with benzene, which was prepared from alcohol, oxalyl chloride, and (diacetoxyiodo)benzene via two steps, depending on reaction conditions.These radicals were also utilized for C-C bond formation with electron-deficient olefins.