[(Z)-5,5,5-trichloropent-2-enyl] carbamate

Base Information

Chemical Name:[(Z)-5,5,5-trichloropent-2-enyl] carbamate
CAS No.:4989-45-1
Molecular Formula:C₆H₈Cl₃NO₂
Molecular Weight:232.494
Hs Code.:
NSC Number:526413
DSSTox Substance ID:DTXSID80419777
Wikidata:Q82230969

Synonyms:NSC526413;4989-45-1;DTXSID80419777;NSC-526413

Suppliers and Price of [(Z)-5,5,5-trichloropent-2-enyl] carbamate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 6 raw suppliers

Chemical Property of [(Z)-5,5,5-trichloropent-2-enyl] carbamate

Chemical Property:

Vapor Pressure:2.34E-05mmHg at 25°C
Boiling Point:359.7°Cat760mmHg
Flash Point:171.3°C
Density:1.43g/cm³
XLogP3:2.2
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:230.962062
Heavy Atom Count:12
Complexity:176

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C(C=CCOC(=O)N)C(Cl)(Cl)Cl
Isomeric SMILES:C(/C=C\COC(=O)N)C(Cl)(Cl)Cl

Technology Process of [(Z)-5,5,5-trichloropent-2-enyl] carbamate

There total 5 articles about [(Z)-5,5,5-trichloropent-2-enyl] carbamate 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:

: 4989-44-0
Chlorameisensaeure-<5,5,5-trichlor-pent-2-enylester>

: 4989-45-1
Carbamidsaeure-<5,5,5-trichlor-pent-2-enylester>

Guidance literature:: With ammonia; In tetrachloromethane;
DOI:10.1021/jo01057a020

Reference yield:

: 4954-44-3
1-bromo-5,5,5-trichloro-pent-2-ene

: 4989-45-1
Carbamidsaeure-<5,5,5-trichlor-pent-2-enylester>

Guidance literature:: Multi-step reaction with 4 steps

1: acetic acid

2: HCl / methanol

4: NH₃ / CCl₄

With hydrogenchloride; ammonia; In methanol; tetrachloromethane; acetic acid;
DOI:10.1021/jo01057a020