Acetonitrile, [(diphenylmethyl)amino]-

Base Information

Chemical Name:Acetonitrile, [(diphenylmethyl)amino]-
CAS No.:146495-24-1
Molecular Formula:C15H14N2
Molecular Weight:222.29
Hs Code.:
DSSTox Substance ID:DTXSID30464050
Nikkaji Number:J1.190.198K
Wikidata:Q82289228
Mol file:146495-24-1.mol

Synonyms:Acetonitrile, [(diphenylmethyl)amino]-;146495-24-1;SCHEMBL13185942;DTXSID30464050;AKOS009132299

Suppliers and Price of Acetonitrile, [(diphenylmethyl)amino]-

Supply Marketing:

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

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Chemical Property of Acetonitrile, [(diphenylmethyl)amino]-

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:222.115698455
Heavy Atom Count:17
Complexity:235

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(C2=CC=CC=C2)NCC#N

Technology Process of Acetonitrile, [(diphenylmethyl)amino]-

There total 44 articles about Acetonitrile, [(diphenylmethyl)amino]- 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: 98.0%

: 91-00-9
Benzhydrylamine

: 590-17-0
cyanomethyl bromide

: 146495-24-1
N-(diphenylmethylene)aminoacetonitrile

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 15h;
DOI:10.1055/s-2000-6428

Reference yield: 95.0%

: 107-14-2
chloroacetonitrile

: 91-00-9
Benzhydrylamine

: 146495-24-1
N-(diphenylmethylene)aminoacetonitrile

Guidance literature:: With tetra-(n-butyl)ammonium iodide; N-ethyl-N,N-diisopropylamine; In acetonitrile; at 20 ℃; for 72h; Inert atmosphere;
DOI:10.1016/j.tetasy.2012.11.010

Reference yield: 88.0%

: 119072-55-8,7188-38-7
tert-butylisonitrile

: C₂₃H₂₀N₂O₂

: 371-40-4
4-fluoroaniline

: N-(2-(tert-butylamino)-2-oxoethyl)-N-(4-fluorophenyl)benzamide

: 146495-24-1
N-(diphenylmethylene)aminoacetonitrile

Guidance literature:: With hydrogenchloride; iron(II) acetate; In 1,4-dioxane; water; at 90 ℃; for 12h; Inert atmosphere;
DOI:10.1039/d1cc03348d