2-Chloroethyl carbamate

2-Chloroethyl carbamate Suppliers list
Company Name: Shanghai AmasPharm Co., Ltd.  
Tel: 021-54540637 18621091017
Email: sales@amaspharm.com
Company Name: ZhengZhou HuaWen Chemical Co.Ltd  
Tel: 0370-2785118 17550508557
Email: 675141927@qq.com
Company Name: Finetech Industry Limited  
Tel: 027-87465837 19945049750
Email: sales@finetechnology-ind.com
Company Name: Shanghai Changyan Chem & Tech Co., Ltd.  
Tel: 021-20242659 18930833303
Email: sales@changyanchem.cn
Company Name: Shanghai CR Corporation Limited  
Tel: 13917420128 13062833949
Email: fred.wen@crcorporation.cn

2-Chloroethyl carbamate manufacturers

2-Chloroethyl carbamate Basic information
Synthesis Uses
Product Name:2-Chloroethyl carbamate
Synonyms:B-CHLOROETHYL CARBAMATE;BETA-CHLOROETHYLURETHANE;BETA-CHLOROETHYL CARBAMATE;2-CHLOROETHYL CARBAMATE;2-CHLOROETHYL CARBAMATE 97%;Carbamic acid, beta-chloroethyl ester;carbamicacid,2-chloroethylester;carbamicacid,beta-chloroethylester
CAS:2114-18-3
MF:C3H6ClNO2
MW:123.54
EINECS:218-310-1
Product Categories:
Mol File:2114-18-3.mol
2-Chloroethyl carbamate Structure
2-Chloroethyl carbamate Chemical Properties
Melting point 74-77 °C(lit.)
Boiling point 264.3±23.0 °C(Predicted)
density 1.2776 (rough estimate)
refractive index 1.5000 (estimate)
pka13.18±0.50(Predicted)
InChIInChI=1S/C3H6ClNO2/c4-1-2-7-3(5)6/h1-2H2,(H2,5,6)
InChIKeyLIJLYNWYKULUHA-UHFFFAOYSA-N
SMILESC(OC(=O)N)CCl
CAS DataBase Reference2114-18-3(CAS DataBase Reference)
NIST Chemistry ReferenceCarbamic acid, 2-chloroethyl ester(2114-18-3)
EPA Substance Registry System2-Chloroethyl carbamate (2114-18-3)
Safety Information
Hazard Codes Xn
Risk Statements 22-36/37/38
Safety Statements 36/37/39-45
WGK Germany 3
RTECS EZ1475000
TSCA TSCA listed
MSDS Information
ProviderLanguage
SigmaAldrich English
2-Chloroethyl carbamate Usage And Synthesis
Synthesis

Using chloroethanol and a carbamylated reagent as raw materials, 2-chloroethylcarbamate is produced in a one-step reaction in the presence of a catalyst. The specific process is as follows:
In a 1000ml four-necked round-bottom flask equipped with a reflux condenser and an electric stirrer, 563.5g (7mol) of chloroethanol is added, the stirring is started, and the temperature is raised. When the temperature reaches 90℃, 307.5g of urea nitrate (2.5mol) and 172.5g of sodium nitrite (1mol) are added. The reaction is carried out between 80-125℃ for 4 hours. Excess chloroethanol is distilled off, and 500ml of diethyl ether is added to the residue. After thorough stirring, the mixture is filtered, and the diethyl ether is distilled off. 2-chloroethylcarbamate is then distilled off under reduced pressure, yielding 90g, with a yield of 30%.


Synthesis of 2114-18-3

Uses2-Chloroethylcarbamate, also known as chloroethyl carbamate, is a synthetic intermediate of carbachol. Carbachol is a complete cholinergic drug, which is significantly effective in treating glaucoma and postpartum abdominal distension and urinary retention.
2-Chloroethyl carbamate Preparation Products And Raw materials
Tag:2-Chloroethyl carbamate(2114-18-3) Related Product Information
Polyurethane Chlorpropham Dithiooxamide Estramustine TERT-BUTYL BIS(2-CHLOROETHYL)CARBAMATE estra-1,3,5(10)-triene-3,17beta-diol 3-[bis(2-chloroethyl)carbamate] 17-(dihydrogen phosphate) Formic acid Estramustine sodium phosphate 1-Chloromethyl-2-chloroethyl=carbamate 4-nitrophenyl-N-(2-chloroethyl)carbamate ethyl N,N-bis(2-chloroethyl)carbamate 2-Chloroethyl carbamate Amino formate herbicide 17-oxo-5-androsten-3beta-yl-N,N-bis(2'-chloroethyl)carbamate 17-O-((2-(3-(4-azido-3-iodophenyl)propionamido)ethyl)carbamyl)estradiol-3-N-bis(chloroethyl)carbamate Estra 1,3,5 (10)-Triene 3,17-Diol-3 [Bis(2-Chloroethyl)Carbamate]-17-Phosphate 1,3,5(10)-Estratriene-3,17β-diol 3-[bis(2-chloroethyl)carbamate]17-(methylamino)acetate dihydrotestosterone-17-N-bis(2-chloroethyl)carbamate