Benzamide, N-(3-cyano-4,5-dihydro-2-furanyl)-

Base Information

Chemical Name:Benzamide, N-(3-cyano-4,5-dihydro-2-furanyl)-
CAS No.:98061-56-4
Molecular Formula:C12H10N2O2
Molecular Weight:214.224
Hs Code.:
DSSTox Substance ID:DTXSID00428866
Nikkaji Number:J602.733D
Wikidata:Q82241701

Synonyms:98061-56-4;N-(3-Cyano-4,5-dihydrofuran-2-yl)benzamide;Benzamide, N-(3-cyano-4,5-dihydro-2-furanyl)-;DTXSID00428866;2-benzoylamino-3-cyano-4,5-dihydrofuran

Suppliers and Price of Benzamide, N-(3-cyano-4,5-dihydro-2-furanyl)-

Supply Marketing:

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

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Chemical Property of Benzamide, N-(3-cyano-4,5-dihydro-2-furanyl)-

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:214.074227566
Heavy Atom Count:16
Complexity:359

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1COC(=C1C#N)NC(=O)C2=CC=CC=C2

Technology Process of Benzamide, N-(3-cyano-4,5-dihydro-2-furanyl)-

There total 1 articles about Benzamide, N-(3-cyano-4,5-dihydro-2-furanyl)- 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: 81.0%

: 27512-24-9
2-amino-4,5-dihydro-3-furancarbonitrile

: 98-88-4
benzoyl chloride

: 98061-56-4
2-benzamido-4,5-dihydro-3-furancarbonitrile

Guidance literature:: In pyridine; at 50 ℃; for 2h;

Reference yield: 82.0%

: 98061-56-4
2-benzamido-4,5-dihydro-3-furancarbonitrile

: 133036-73-4
N-benzoyl-4-chloro-2-cyanobutanamide

Guidance literature:: With titanium tetrachloride; In chloroform; for 1h; Product distribution; Mechanism; Heating; other 2-acylamino-4,5-dihydro-3-furancarbonitriles;