Furan, 2-(2-nitro-1-propenyl)-

Base Information

Chemical Name:Furan, 2-(2-nitro-1-propenyl)-
CAS No.:33322-20-2
Molecular Formula:C7H7 N O3
Molecular Weight:153.137
Hs Code.:2932190090
NSC Number:35560
Nikkaji Number:J1.014.927D
Wikidata:Q76325852
Mol file:33322-20-2.mol

Synonyms:2-(2-nitro-1-propenyl)furan;UC 244;UC-244

Suppliers and Price of Furan, 2-(2-nitro-1-propenyl)-

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

Matrix Scientific
2-(2-Nitroprop-1-en-1-yl)furan 95%+
10g
$ 1548.00

AccelPharmtech
2-(2-nitro-1-propen-1-yl)-Furan 97.00%
25G
$ 3120.00

AccelPharmtech
2-(2-nitro-1-propen-1-yl)-Furan 97.00%
5G
$ 1700.00

AccelPharmtech
2-(2-nitro-1-propen-1-yl)-Furan 97.00%
1G
$ 1530.00

Total 7 raw suppliers

Chemical Property of Furan, 2-(2-nitro-1-propenyl)-

Chemical Property:

Vapor Pressure:0.105mmHg at 25°C
Boiling Point:229.5°Cat760mmHg
Flash Point:92.6°C
PSA：58.96000
Density:1.217g/cm³
LogP:2.44030
XLogP3:2
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:1
Exact Mass:153.042593085
Heavy Atom Count:11
Complexity:183

Purity/Quality:

97% ^*data from raw suppliers

2-(2-Nitroprop-1-en-1-yl)furan 95%+ ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CC1=CC=CO1)[N+](=O)[O-]
Isomeric SMILES:C/C(=C/C1=CC=CO1)/[N+](=O)[O-]

Technology Process of Furan, 2-(2-nitro-1-propenyl)-

There total 2 articles about Furan, 2-(2-nitro-1-propenyl)- 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: 96.0%

: 98-01-1
furfural

: 79-24-3
Nitroethane

: 33322-20-2
2-(2-methyl-2-nitrovinyl)-furan

Guidance literature:: With (2-hydroxyethyl)ammonium formate; at 20 ℃; for 1.2h; Ionic liquid;
DOI:10.1021/jo101696z

Reference yield: 69.0%

: 79-24-3
Nitroethane

: 617-89-0
furan-2-ylmethanamine

: 33322-20-2
2-(2-methyl-2-nitrovinyl)-furan

Guidance literature:: With 4-(4-fluorophenyl)naphthalene-1,2-dione; oxygen; at 80 ℃; for 12h;
DOI:10.1021/acscatal.9b03442

Reference yield: 98.0%

: 33322-20-2
2-(2-methyl-2-nitrovinyl)-furan

: 1195694-52-0
4-methyl-N-(2-((E)-3-oxo-3-phenylprop-1-en-1-yl)phenyl)benzenesulfonamide

: 2-[(2R,3S,4R)-2-(2-furyl)-1,2,3,4-tetrahydro-3-methyl-3-nitro-1-tosyl-4-quinolinyl]-1-phenylethanone

Guidance literature:: 2-(2-methyl-2-nitrovinyl)-furan; With 3-((3,5-bis(trifluoromethyl)phenyl)amino)-4-(((S)-(6-methoxyquinoline-4-yl))((1S,2S,4S,5R-5-vinylquinuclidine-2-yl)methyl)amino)cyclobutan-3-ene-1,2-dione; In 1,2-dichloro-ethane; toluene; at 20 ℃; for 0.166667h;

4-methyl-N-(2-((E)-3-oxo-3-phenylprop-1-en-1-yl)phenyl)benzenesulfonamide; In 1,2-dichloro-ethane; toluene; at 20 ℃; for 24h; enantioselective reaction;
DOI:10.1002/adsc.201300670