2-Chloroethyl 3,4-dichlorophenylcarbamate

Base Information

• Chemical Name: 2-Chloroethyl 3,4-dichlorophenylcarbamate
• CAS No.: 25217-34-9
• Molecular Formula: C9H8Cl3NO2
• Molecular Weight: 268.5243
• European Community (EC) Number: 665-619-6
• NSC Number: 135722
• DSSTox Substance ID: DTXSID80948072
• Wikidata: Q82925864
• Mol file: 25217-34-9.mol

Synonyms:25217-34-9;NSC135722;DTXSID80948072;AKOS024334497;NSC-135722;2-chloroethyl 3,4-dichlorophenylcarbamate;2-Chloroethyl hydrogen (3,4-dichlorophenyl)carbonimidate

Chemical Property of 2-Chloroethyl 3,4-dichlorophenylcarbamate

Chemical Property:

• Vapor Pressure: 0.000484mmHg at 25°C
• Boiling Point: 313.8°C at 760 mmHg
• Flash Point: 143.6°C
• Density: 1.486g/cm³
• XLogP3: 4.1
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 4
• Exact Mass: 266.962062
• Heavy Atom Count: 15
• Complexity: 216

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C1=CC(=C(C=C1NC(=O)OCCCl)Cl)Cl

Technology Process of 2-Chloroethyl 3,4-dichlorophenylcarbamate

There total 1 articles about 2-Chloroethyl 3,4-dichlorophenylcarbamate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ 3,4-Dichlor-carbanilsaeure-2-chlor-aethylester (25217-34-9)

Guidance literature:

3,4-Dichlor-phenylisocyanat, CH2Cl-CH2-OH;

DOI:10.1021/jm00341a006

Reference yield:

3,4-Dichlor-carbanilsaeure-2-chlor-aethylester (25217-34-9) → N-(3,4-dichlorophenyl)oxazolidin-2-one (90273-45-3)

Guidance literature:

With sodium hydroxide;

DOI:10.1021/jo01056a022

Downstream raw materials:

N-(3,4-dichlorophenyl)oxazolidin-2-one