6092-47-3

Basic information

• Product Name: N-CHLOROACETYL URETHANE
• Synonyms: N-2-CHLOROACETYLURETHANE;N-CHLOROACETYL URETHANE;TIMTEC-BB SBB003907;n-chloroacetyl carbamic acid ethyl ester;N-Chloroacetyl urethane,98%;Ethyl (chloroacetyl)carbamate;ethyl N-(2-chloroacetyl)carbamate;ethyl N-(2-chloroethanoyl)carbamate
• CAS NO: 6092-47-3
• Molecular Formula: C₅H₈ClNO₃
• Molecular Weight: 165.57
• Mol File: 6092-47-3.mol
• Article Data: 1

Chemical Properties

• Melting Point: 126-131 °C
• Appearance: White to off-white/Crystalline Powder With Hue
• Density: 1.3761 (rough estimate)
• Refractive Index: 1.5810 (estimate)
• PKA: 7.48±0.46(Predicted)
• CAS DataBase Reference: N-CHLOROACETYL URETHANE(CAS DataBase Reference)
• NIST Chemistry Reference: N-CHLOROACETYL URETHANE(6092-47-3)
• EPA Substance Registry System: N-CHLOROACETYL URETHANE(6092-47-3)

Safety Data

• Hazard Codes: Xn
• Statements: 21/22
• Safety Statements: 36/37
• HazardClass: IRRITANT
• Hazardous Substances Data: 6092-47-3(Hazardous Substances Data)

Usage

Chemical Properties

white to off-white crystalline powder with

InChI:InChI=1/C5H8ClNO3/c1-2-10-5(9)7-4(8)3-6/h2-3H2,1H3,(H,7,8,9)

Upstream product

• 79-04-9 chloroacetyl chloride 
• 51-79-6 urethane 
• 105-39-5 chloroacetic acid ethyl ester 
• 79-37-8 oxalyl dichloride 
• 64-17-5 ethanol 
• 79-07-2 Chloroacetamide 
• 4461-30-7 2-chloroacetylisocyanate 

Downstream Products

• 32549-33-0 1-(4-chlorophenyl)imidazolidine-2,4-dione 
• 41526-30-1 1-(4-methoxyphenyl)hydantoin 
• 32549-32-9 1-(3-methylphenyl)hydantoin 
• 60984-45-4 1-o-tolyl-imidazolidine-2,4-dione 
• 32549-34-1 1-(4-Bromophenyl)imidazolidine-2,4-dione 
• 79-07-2 Chloroacetamide 
• 1005785-69-2 ethyl (6-iodoimidazo[1,2-b]pyridazin-2-yl)carbamate 
• 34392-97-7 3-(4-methylbenzyl)-2-thioxothiazolidin-4-one 
• 865604-27-9 (7-chloro-imidazo[1,2-c]pyrimidin-2-yl)-carbamic acid ethyl ester 
• 87789-27-3 (4-Amino-2-benzylsulfanyl-thiazole-5-carbonyl)-carbamic acid ethyl ester 
• 29163-29-9 Phenyl-phosphonodithioic acid S-(2-ethoxycarbonylamino-2-oxo-ethyl) ester O-methyl ester 

Relevant articles and documents

A concise approach to n-substituted rhodanines through a base-assisted one-pot coupling and cyclization process

An efficient approach to obtain functionalized rhodanines was developed through a base-assisted one-pot coupling and continuous cyclization of a primary amine, carbon disulfide, and methyl (2-chloroacetyl)carbamate. This conversion tolerates a broad range of functional groups and can be used to scale the preparation of N-substituted rhodanines in excellent yields.