4-(2-Furyl)-4-oxobutanenitrile

Base Information

Chemical Name:4-(2-Furyl)-4-oxobutanenitrile
CAS No.:17960-37-1
Molecular Formula:C8H7 N O2
Molecular Weight:149.149
Hs Code.:2932190090
European Community (EC) Number:850-577-5
DSSTox Substance ID:DTXSID80366474
Nikkaji Number:J3.489.506F
Wikidata:Q82151699
Mol file:17960-37-1.mol

Synonyms:4-(2-furyl)-4-oxobutanenitrile;4-(furan-2-yl)-4-oxobutanenitrile;17960-37-1;HMS1718H19;SCHEMBL11218386;DTXSID80366474;4-Oxo-4-(2-furyl)butanenitrile;MFCD00126351;AKOS000118573;CS-0230050;EN300-10208;Z57000489

Suppliers and Price of 4-(2-Furyl)-4-oxobutanenitrile

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

TRC
4-(furan-2-yl)-4-oxobutanenitrile
50mg
$ 155.00

American Custom Chemicals Corporation
4-(2-FURYL)-4-OXOBUTANENITRILE 95.00%
5G
$ 1928.08

American Custom Chemicals Corporation
4-(2-FURYL)-4-OXOBUTANENITRILE 95.00%
2.5G
$ 1473.14

American Custom Chemicals Corporation
4-(2-FURYL)-4-OXOBUTANENITRILE 95.00%
1G
$ 983.52

AK Scientific
4-(2-Furyl)-4-oxobutanenitrile
1g
$ 905.00

Total 3 raw suppliers

Chemical Property of 4-(2-Furyl)-4-oxobutanenitrile

Chemical Property:

Vapor Pressure:0.000229mmHg at 25°C
Boiling Point:325.5°Cat760mmHg
Flash Point:150.7°C
PSA：54.00000
Density:1.145g/cm³
LogP:1.76608
XLogP3:0.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:149.047678466
Heavy Atom Count:11
Complexity:192

Purity/Quality:

97% ^*data from raw suppliers

4-(furan-2-yl)-4-oxobutanenitrile ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=COC(=C1)C(=O)CCC#N

Technology Process of 4-(2-Furyl)-4-oxobutanenitrile

There total 11 articles about 4-(2-Furyl)-4-oxobutanenitrile 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: 83.0%

: 107-14-2
chloroacetonitrile

: 111886-29-4
tert-butyldimethyl((1-(furan-2-yl)vinyl)oxy)silane

: 17960-37-1
4-(furan-2-yl)-4-oxobutanenitrile

Guidance literature:: chloroacetonitrile; tert-butyldimethyl((1-(furan-2-yl)vinyl)oxy)silane; With 2,6-dimethylpyridine; potassium 5-bromo-1H-indole-1-carbodithioate; In acetonitrile; at 25 ℃; for 24h; Schlenk technique; Inert atmosphere; Irradiation;

With trifluoroacetic acid; In chloroform; acetonitrile; Schlenk technique; Inert atmosphere;
DOI:10.1002/anie.201915814

Reference yield: 78.0%

: 81331-50-2
S-(2-pyridinyl) furan-2-carbothioate

: 107-13-1,25014-41-9
acrylonitrile

: 17960-37-1
4-(furan-2-yl)-4-oxobutanenitrile

Guidance literature:: With C₅₃H₇₄CoN₅O₁₅⁽¹⁺⁾*ClO₄^(1-)*H₂O; ammonium chloride; zinc; In acetonitrile; at 19 - 25 ℃; for 16h; Sealed tube; Inert atmosphere; Irradiation;
DOI:10.1002/adsc.201700913

Reference yield: 30.0%

: 98-01-1
furfural

: 64-17-5
ethanol

: 17960-37-1
4-(furan-2-yl)-4-oxobutanenitrile

: 614-99-3
Ethyl 2-furoate

: 492-94-4
furil

: 552-86-3
furoin

Guidance literature:: With 3,4-dimethyl-5-<2-(methylsulfinyl)ethyl>thiazolium chloride; triethylamine; acrylonitrile; Further byproducts given;