2-Isobutoxyphenol

Base Information

Chemical Name:2-Isobutoxyphenol
CAS No.:21315-20-8
Molecular Formula:C₁₀H₁₄O₂
Molecular Weight:166.22
Hs Code.:2909500090
DSSTox Substance ID:DTXSID70351117
Nikkaji Number:J364.662I
Wikidata:Q82127275
Mol file:21315-20-8.mol

Synonyms:2-isobutoxyphenol;21315-20-8;2-(2-methylpropoxy)phenol;2-(2-Methylpropyloxy)phenol;ghl.PD_Mitscher_leg0.605;o-isobutoxyphenol;TimTec1_005338;SCHEMBL77820;DTXSID70351117;PBVUSKGIFXCUMR-UHFFFAOYSA-N;HMS1549C14;MFCD00474627;STK753188;AKOS005615677;BS-36809;CS-0316343

Suppliers and Price of 2-Isobutoxyphenol

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
2-isobutoxyphenol
50mg
$ 45.00

Crysdot
2-Isobutoxyphenol 95+%
5g
$ 339.00

ChemBridge Corporation
2-isobutoxyphenol 95%
1 g
$ 70.00

American Custom Chemicals Corporation
2-ISOBUTOXYPHENOL 95.00%
5G
$ 1138.78

American Custom Chemicals Corporation
2-ISOBUTOXYPHENOL 95.00%
1G
$ 721.59

Total 5 raw suppliers

Chemical Property of 2-Isobutoxyphenol

Chemical Property:

Vapor Pressure:0.0154mmHg at 25°C
Melting Point:50-51 °C
Boiling Point:248.4°C at 760 mmHg
PKA:9?+-.0.30(Predicted)
Flash Point:95.3°C
Density:1.027g/cm³
XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:166.099379685
Heavy Atom Count:12
Complexity:123

Purity/Quality:

99% ^*data from raw suppliers

2-isobutoxyphenol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(C)COC1=CC=CC=C1O

Technology Process of 2-Isobutoxyphenol

There total 6 articles about 2-Isobutoxyphenol 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: 80.0%

: 513-38-2
Isobutyl iodide

: 120-80-9,19481-10-8,37349-32-9
benzene-1,2-diol

: 21315-20-8
2-isobutoxyphenol

Guidance literature:: With potassium carbonate; In acetone; for 72h; Reflux;
DOI:10.1016/j.tet.2011.06.013

Reference yield:

: 81995-32-6
2-(i-butoxy)benzaldehyde

: 21315-20-8
2-isobutoxyphenol

Guidance literature:: Multi-step reaction with 2 steps

1: 30percent aq. H₂O₂ / 2-NO₂C₆H₄SeSeC₆H₄NO₂-2 / CH₂Cl₂ / 31 h / Ambient temperature

2: KOH / methanol / 1 h / Ambient temperature

With potassium hydroxide; dihydrogen peroxide; bis(o-nitrophenyl) diselenide; In methanol; dichloromethane;
DOI:10.1055/s-1989-27183

Reference yield:

: 90-02-8
salicylaldehyde

: 21315-20-8
2-isobutoxyphenol

Guidance literature:: Multi-step reaction with 3 steps

1: K₂CO₃ / acetone / Heating

2: 30percent aq. H₂O₂ / 2-NO₂C₆H₄SeSeC₆H₄NO₂-2 / CH₂Cl₂ / 31 h / Ambient temperature

3: KOH / methanol / 1 h / Ambient temperature

With potassium hydroxide; dihydrogen peroxide; potassium carbonate; bis(o-nitrophenyl) diselenide; In methanol; dichloromethane; acetone;
DOI:10.1055/s-1989-27183