Ethanimidoyl chloride, 2,2,2-trifluoro-N-(phenylmethyl)-

Base Information

Chemical Name:Ethanimidoyl chloride, 2,2,2-trifluoro-N-(phenylmethyl)-
CAS No.:88708-70-7
Molecular Formula:C9H7ClF3N
Molecular Weight:221.609
Hs Code.:
DSSTox Substance ID:DTXSID20472346
Nikkaji Number:J519.482B

Synonyms:Ethanimidoyl chloride, 2,2,2-trifluoro-N-(phenylmethyl)-;88708-70-7;SCHEMBL7763107;DTXSID20472346;ZSRKHHOFCRGTQX-UHFFFAOYSA-N;N-benzyltrifluoroacetimidoyl chloride;AKOS030596078;BB 0322712;N-benzyl-2,2,2-trifluoroethanimidoyl chloride;(1E)-2,2,2-trifluoro-N-[(E)-phenylmethyl]ethanimidoyl chloride

Suppliers and Price of Ethanimidoyl chloride, 2,2,2-trifluoro-N-(phenylmethyl)-

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 1 raw suppliers

Chemical Property of Ethanimidoyl chloride, 2,2,2-trifluoro-N-(phenylmethyl)-

Chemical Property:

XLogP3:3.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:221.0219114
Heavy Atom Count:14
Complexity:207

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C=C1)CN=C(C(F)(F)F)Cl

Technology Process of Ethanimidoyl chloride, 2,2,2-trifluoro-N-(phenylmethyl)-

There total 1 articles about Ethanimidoyl chloride, 2,2,2-trifluoro-N-(phenylmethyl)- 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:

: 100-46-9
benzylamine

: 88708-70-7
N-benzyl-2,2,2-trifluoroacetimidoyl chloride

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 20 °C / Cooling with ice

2: triphenylphosphine; tetrachloromethane / dichloromethane / 3 h / 60 °C / Glovebox

With tetrachloromethane; triethylamine; triphenylphosphine; In dichloromethane; 2: |Appel Halogenation;
DOI:10.1055/a-1681-3972