2-(But-3-en-2-yl)-6-nitrophenol

Base Information

Chemical Name:2-(But-3-en-2-yl)-6-nitrophenol
CAS No.:31225-05-5
Molecular Formula:C10H11NO3
Molecular Weight:193.202
Hs Code.:
DSSTox Substance ID:DTXSID50490634
Mol file:31225-05-5.mol

Synonyms:31225-05-5;SCHEMBL426968;DTXSID50490634;HLYVXHPHLRDLSM-UHFFFAOYSA-N;2-(But-3-en-2-yl)-6-nitrophenol;2-(1-Methyl-2-propen-1-yl)-6-nitrophenol

Suppliers and Price of 2-(But-3-en-2-yl)-6-nitrophenol

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
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Total 0 raw suppliers

Chemical Property of 2-(But-3-en-2-yl)-6-nitrophenol

Chemical Property:

Boiling Point:88 °C(Press: 0.35 Torr)
PSA：66.05000
Density:1?+-.0.06 g/cm3(Predicted)
LogP:3.11310
XLogP3:3.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:193.07389321
Heavy Atom Count:14
Complexity:224

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(C=C)C1=C(C(=CC=C1)[N+](=O)[O-])O

Technology Process of 2-(But-3-en-2-yl)-6-nitrophenol

There total 3 articles about 2-(But-3-en-2-yl)-6-nitrophenol 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: 16.0%

: (Z)-2-buten-1-yl 2-nitrophenyl ether

: 107616-14-8
(E)-1-(but-2-en-1-yloxy)-2-nitrobenzene

: 31225-05-5
2-(1-methyl-2-propen-1-yl)-6-nitrophenol

Guidance literature:: at 200 ℃; for 5h;

Reference yield:

: 88-75-5,78813-12-4
2-hydroxynitrobenzene

: 31225-05-5
2-(1-methyl-2-propen-1-yl)-6-nitrophenol

Guidance literature:: Multi-step reaction with 2 steps

1: K₂CO₃ / acetone

2: decahydronaphthalene / 150 - 160 °C

With potassium carbonate; In acetone; decalin;