2-Phenoxyethyl chloroformate

Base Information

• Chemical Name: 2-Phenoxyethyl chloroformate
• CAS No.: 34743-87-8
• Molecular Formula: C9H9ClO3
• Molecular Weight: 200.622
• Hs Code.: 2915900090
• European Community (EC) Number: 252-180-7
• DSSTox Substance ID: DTXSID20188298
• Nikkaji Number: J250.966K
• Wikidata: Q72501023
• Mol file: 34743-87-8.mol

Synonyms:2-Phenoxyethyl chloroformate;34743-87-8;2-phenoxyethyl carbonochloridate;EINECS 252-180-7;Carbonochloridic acid, 2-phenoxyethyl ester;2-phenoxyethylcarbonochloridate;SCHEMBL2389740;DTXSID20188298;MFCD00673041;AKOS015890579;carbonochloridic acid 2-phenoxyethyl ester;Chloridocarbonic acid 2-phenoxyethyl ester;FT-0659363;EN300-1612351;A822379;J-510236;(S)-(-)-2-(DIPHENYLPHOSPHORYL)-2-ETHYL-1,1-BINAPHTHYL

Chemical Property of 2-Phenoxyethyl chloroformate

Chemical Property:

• Vapor Pressure: 0.00334mmHg at 25°C
• Melting Point: 28oC
• Refractive Index: 1.517
• Boiling Point: 282.5 °C at 760 mmHg
• Flash Point: 120.1 °C
• PSA: 35.53000
• Density: 1.243 g/cm³
• LogP: 2.44080
• XLogP3: 2.8
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 5
• Exact Mass: 200.0240218
• Heavy Atom Count: 13
• Complexity: 155

Purity/Quality:

99% ^*data from raw suppliers

2-PhenoxyethylChloroformate ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of 2-Phenoxyethyl chloroformate

There total 4 articles about 2-Phenoxyethyl chloroformate 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:

phosgene (75-44-5) + 2-Phenoxyethanol (122-99-6,56257-90-0,9004-78-8) → 1-chlorocarbonyloxy-2-phenoxy-ethane (34743-87-8)

Guidance literature:

Reference yield:

phosgene (75-44-5) + 2-Phenoxyethanol (122-99-6,56257-90-0,9004-78-8) → bis(2-phenoxyethyl)carbonate (22855-36-3) + 1-chlorocarbonyloxy-2-phenoxy-ethane (34743-87-8)

Guidance literature:

at 35 - 40 ℃;

Reference yield:

2-Phenoxyethanol (122-99-6,56257-90-0,9004-78-8) → 1-chlorocarbonyloxy-2-phenoxy-ethane (34743-87-8)

Guidance literature:

upstream raw materials:

phosgene

2-Phenoxyethanol

Downstream raw materials:

carbonic acid-(5-acetyl-[8]quinolyl ester)-(2-phenoxy-ethyl ester)

2-chloroethoxybenzene

OO-(3-hydroxy-1,1-dimethylbutyl) O-(2-phenoxyethyl) monoperoxycarbonate

N'-Phenyl-hydrazinecarboxylic acid 2-phenoxy-ethyl ester

Refernces

• 1、 -. "(2-Aryl-4-phenylthioalkyl-1,3-dioxolan-2-ylmethyl)azole derivatives". . . Retrieved 2008/06/13.