2,3,3-Triphenylacrylonitrile

Base Information

Chemical Name:2,3,3-Triphenylacrylonitrile
CAS No.:6304-33-2
Molecular Formula:C21H15 N
Molecular Weight:281.357
Hs Code.:2926909090
European Community (EC) Number:228-610-4
NSC Number:42900
DSSTox Substance ID:DTXSID60212329
Nikkaji Number:J33.777C
Wikidata:Q27115912
ChEMBL ID:CHEMBL305168
Mol file:6304-33-2.mol

Synonyms:2,3,3-triphenylacrylonitrile

Suppliers and Price of 2,3,3-Triphenylacrylonitrile

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

Alfa Aesar
Triphenylacrylonitrile, 98+%
5g
$ 58.80

American Custom Chemicals Corporation
TRIPHENYLACRYLONITRILE 95.00%
5G
$ 865.78

Total 11 raw suppliers

Chemical Property of 2,3,3-Triphenylacrylonitrile

Chemical Property:

Vapor Pressure:1.04E-06mmHg at 25°C
Melting Point:165-167°C
Refractive Index:1.8240 (estimate)
Boiling Point:403.2°C at 760 mmHg
Flash Point:198.9°C
PSA：23.79000
Density:1.114g/cm³
LogP:5.16928
XLogP3:5.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:281.120449483
Heavy Atom Count:22
Complexity:400

Purity/Quality:

97% ^*data from raw suppliers

Triphenylacrylonitrile, 98+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Statements: 20/22-36/37/38
Safety Statements: 22-36/37/39

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=C(C2=CC=CC=C2)C3=CC=CC=C3)C#N

Technology Process of 2,3,3-Triphenylacrylonitrile

There total 26 articles about 2,3,3-Triphenylacrylonitrile 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%

: 1607-57-4
Triphenylvinyl bromide

: 105-56-6
ethyl 2-cyanoacetate

: 6304-33-2
2,3,3-triphenylacrylonitrile

Guidance literature:: Triphenylvinyl bromide; With copper(I) oxide; oxygen; triphenylphosphine; In 1-methyl-pyrrolidin-2-one; Schlenk technique; Sealed tube;

ethyl 2-cyanoacetate; With silver nitrate; acetic acid; In 1-methyl-pyrrolidin-2-one; at 130 ℃; for 18h; Schlenk technique; Sealed tube;
DOI:10.1039/c7nj03405a

Reference yield: 76.0%

: 108-86-1,52753-63-6
bromobenzene

: potassiumhexacyanoferrate(II) trihydrate

: 501-65-5
diphenyl acetylene

: 6304-33-2
2,3,3-triphenylacrylonitrile

Guidance literature:: With palladium diacetate; sodium carbonate; In N,N-dimethyl acetamide; at 120 ℃; for 5h; Inert atmosphere;
DOI:10.1021/ol703018t

Reference yield: 68.0%

: 119-61-9
benzophenone

: 140-29-4
phenylacetonitrile

: 6304-33-2
2,3,3-triphenylacrylonitrile

Guidance literature:: phenylacetonitrile; With sodium hydride; In tetrahydrofuran; mineral oil; at 40 ℃; for 2h;

benzophenone; In tetrahydrofuran; mineral oil; for 6h; Reflux;
DOI:10.1039/c3ra23188g