110175-83-2

Basic information

• Product Name: (carbonic acid ethyl ester)-(4-nitro-benzoic acid )-anhydride
• Synonyms: (carbonic acid ethyl ester)-(4-nitro-benzoic acid )-anhydride
• CAS NO: 110175-83-2
• Molecular Weight: 239.185
• Mol File: 110175-83-2.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (carbonic acid ethyl ester)-(4-nitro-benzoic acid )-anhydride(CAS DataBase Reference)
• NIST Chemistry Reference: (carbonic acid ethyl ester)-(4-nitro-benzoic acid )-anhydride(110175-83-2)
• EPA Substance Registry System: (carbonic acid ethyl ester)-(4-nitro-benzoic acid )-anhydride(110175-83-2)

Safety Data

• Hazardous Substances Data: 110175-83-2(Hazardous Substances Data)

Upstream product

• 541-41-3 chloroformic acid ethyl ester 
• 62-23-7 4-nitro-benzoic acid 

Downstream Products

• 902-47-6 p-nitrobenzoic anhydride 
• 831-69-6 ethenyl 4-nitrobenzoate 
• 121902-39-4 2-(4-Nitro-phenyl)-1,3,6,9b-tetraaza-phenalene-4-carboxylic acid ethyl ester 
• 121902-47-4 2-(4-Nitro-phenyl)-1,3,6,9b-tetraaza-phenalene 
• 619-73-8 4-nitrobenzyl chloride 
• 121924-13-8 9-Cyano-5-methyl-2-(4-nitro-phenyl)-1,9b-diaza-phenalene-7-carboxylic acid methyl ester 
• 121902-09-8 9-Cyano-2-(4-nitro-phenyl)-1,9b-diaza-phenalene-7-carboxylic acid methyl ester 
• 78476-95-6 2-Cyclohexylamino-4,4-dimethyl-6-(4-nitrobenzoyloxy)-2,5-cyclohexadien-1-on 
• 619-80-7 4-nitrobenzamide 

Relevant articles and documents

Convenient preparation of primary amides via activation of carboxylic acids with ethyl chloroformate and triethylamine under mild conditions

Primary amides were easily prepared in 22-99% yields from the corresponding carboxylic acids 1 or 5 with NH4Cl via activation with ClCO 2Et and Et3N. The enantiomers of the corresponding primary amides of Cbz-, Boc-, or Fmoc-α-amino acids can be separated by using a chiral column.

Selective reduction of mixed anhydrides of carboxylic acids to alcohols using borohydride exchange resin (BER)-nickel acetate

Mixed anhydrides of carboxylic acids have been selectively reduced to alcohols with borohydride exchange resin-nickel acetate under mild conditions and in good yields.

Studies on Quinolizine Derivatives. XXII. Syntheses and Properties of 2-Phenylazacylazine Derivatives

By the reaction of 6-methyl-4-imino-4H-quinolizine derivatives (5, 8) with the mixed anhydrides (6a-h), 2-phenyl-1-azacylazines (7a-p, 9a-g) were obtained. 2-Phenyl-1,3,6-triazacyclazine derivatives (15a-h, 17a-h, 18a-g) were prepared by the