3-Butenamide, N-(2-iodophenyl)-N-(phenylmethyl)-

Base Information

Chemical Name:3-Butenamide, N-(2-iodophenyl)-N-(phenylmethyl)-
CAS No.:879682-42-5
Molecular Formula:C17H16INO
Molecular Weight:377.225
Hs Code.:
DSSTox Substance ID:DTXSID10470992
Nikkaji Number:J2.289.612A
Wikidata:Q82299380

Synonyms:3-Butenamide, N-(2-iodophenyl)-N-(phenylmethyl)-;879682-42-5;DTXSID10470992

Suppliers and Price of 3-Butenamide, N-(2-iodophenyl)-N-(phenylmethyl)-

Supply Marketing:

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

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Chemical Property of 3-Butenamide, N-(2-iodophenyl)-N-(phenylmethyl)-

Chemical Property:

XLogP3:4.2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:377.02766
Heavy Atom Count:20
Complexity:325

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCC(=O)N(CC1=CC=CC=C1)C2=CC=CC=C2I

Technology Process of 3-Butenamide, N-(2-iodophenyl)-N-(phenylmethyl)-

There total 3 articles about 3-Butenamide, N-(2-iodophenyl)-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:

: 615-43-0
2-iodophenylamine

: 879682-42-5
but-3-enoic acid benzyl-(2-iodophenyl)amide

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / sodium cyanoborohydride; zinc(II) chloride / methanol / 2 h / Heating

2: CH₂Cl₂ / 20 °C

With sodium cyanoborohydride; zinc(II) chloride; In methanol; dichloromethane;
DOI:10.1021/jo0522660

Reference yield:

: 100-52-7
benzaldehyde

: 879682-42-5
but-3-enoic acid benzyl-(2-iodophenyl)amide

Guidance literature:: Multi-step reaction with 2 steps

1: 91 percent / sodium cyanoborohydride; zinc(II) chloride / methanol / 2 h / Heating

2: CH₂Cl₂ / 20 °C

With sodium cyanoborohydride; zinc(II) chloride; In methanol; dichloromethane;
DOI:10.1021/jo0522660