49782-76-5

Basic information

• Product Name: Carbonochloridic acid, 3-chlorophenyl ester
• Synonyms: 3-chlorophenyl chloroformate;m-chlorophenyl chloroformate;m-Chlorphenylchlorformiat;Carbonochloridic acid,3-chlorophenyl ester;3-chlorobenzyloxycarbonyl chloride
• CAS NO: 49782-76-5
• Molecular Formula: C7H4Cl2O2
• Molecular Weight: 191.014
• Mol File: 49782-76-5.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Carbonochloridic acid, 3-chlorophenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Carbonochloridic acid, 3-chlorophenyl ester(49782-76-5)
• EPA Substance Registry System: Carbonochloridic acid, 3-chlorophenyl ester(49782-76-5)

Safety Data

• Hazardous Substances Data: 49782-76-5(Hazardous Substances Data)

Upstream product

• 75-44-5 phosgene 
• 108-43-0 3-monochlorophenol 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 3046-27-3 sodium m-chlorophenoxide 

Downstream Products

• 106164-60-7 hexahydro-azepine-1-carboxylic acid-(3-chloro-phenyl ester) 
• 19932-84-4 6-chlorobenzo[d]oxazol-2(3H)-one 
• 13603-93-5 4-chloro-1,3-benzoxazol-2(3H)-one 
• 1202247-79-7 C₁₇H₁₅ClF₃N₃O₂ 
• 1202247-71-9 C₁₆H₁₅Cl₂N₃O₂ 
• 1002100-97-1 C₁₇H₁₅ClN₂O₃ 
• 92847-40-0 N-<4-Hydroxy-butin-(2)-yl>-carbamidsaeure-<3-chlor-phenylester> 
• 92285-90-0 N-<4-Chlor-butin-(2)-yl>-carbamidsaeure-<3-chlor-phenyl>-ester 

Relevant articles and documents

Visible-Light-Induced Intramolecular C(sp2)-H Amination and Aziridination of Azidoformates via a Triplet Nitrene Pathway

Catalytic intramolecular C-H amination and aziridination reactions of o-allylphenyl azidoformates have been achieved under visible-light irradiation, providing a mild, clean, and efficient method for the synthesis of useful benzoxazolones and [5.1.0] bicyclic aziridines. Mechanistic studies suggest that a triplet nitrene acts as the reactive intermediate. The chemoselectivity of the reaction, with alkyl olefin aziridination ? electron deficient olefin aziridination ≈ C(sp2)-H amination ? C(sp3)-H amination was observed, which may be instructive in the development of an understanding of visible-light-induced triplet nitrene transformation reactions.

Synthesis and biological evaluation of piperazinyl carbamates and ureas as fatty acid amide hydrolase (FAAH) and transient receptor potential (TRP) channel dual ligands

The evaluation of a series of piperazinyl carbamates and ureas, designed on the basis of previously reported TRPV1 antagonists and FAAH inhibitors, led to the identification of some 'dual-action' compounds targeting both FAAH and TRPV1 or TRPA1 receptors.

Heat-sensitive recording materials and phenol compounds

Heat-sensitive recording materials contain an electron-donating chromogenic compound and an electron-attracting compound. The recording materials also contain at least one compound represented by the following formula: STR1 wherein R1 and R3 mean a hydrogen atom or an alkyl, aralkyl or aryl group, R2 and R4 denote an alkyl, alkenyl, aralkyl or aryl group, X1, X2, Y1 and Y2 stand for an oxygen or a sulfur atom, and --Z1 -- and --Z2 -- are a specific aromatic group. Also provided are phenol compounds represented by the following formula: STR2 wherein R1, R2, X1 and Y1 have the same meanings as defined above; R5 and R6 are a hydrogen or halogen atom or an alkyl, alkoxy, aralkyl, aryl or hydroxyl group; p and q stand for an integer of 1-4; R5 and R6 may be either the same or different when p and q represent an integer of 2 or greater; and --Z3 -- means a specific divalent group.