3-Methoxy-4-methylphenol

Base Information

Chemical Name:3-Methoxy-4-methylphenol
CAS No.:19217-50-6
Molecular Formula:C8H10O2
Molecular Weight:138.166
Hs Code.:2909500090
European Community (EC) Number:889-836-2
DSSTox Substance ID:DTXSID80568219
Nikkaji Number:J426.334K
Wikidata:Q82454401
Mol file:19217-50-6.mol

Synonyms:3-methoxy-4-methylphenol;19217-50-6;Phenol, 3-methoxy-4-methyl-;MFCD16998731;B-Methoxy-4-methylphenol;SCHEMBL275152;4-methyl-3-(methyloxy)phenol;DTXSID80568219;SOYWOKSOKVRZRZ-UHFFFAOYSA-N;AKOS024048031;AT19376;MB25418;BS-21982;SY224175;CS-0119746;EN300-223951

Suppliers and Price of 3-Methoxy-4-methylphenol

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
3-Methoxy-4-methylphenol
500mg
$ 175.00

Crysdot
3-Methoxy-4-methylphenol 97%
5g
$ 564.00

Apolloscientific
3-Methoxy-4-methylphenol 95%
1g
$ 631.00

Alichem
5-Hydroxy-2-methylanisole
250mg
$ 484.80

Alichem
5-Hydroxy-2-methylanisole
500mg
$ 839.45

Alichem
5-Hydroxy-2-methylanisole
1g
$ 1549.60

AK Scientific
3-Methoxy-4-methylphenol
1g
$ 1275.00

Total 18 raw suppliers

Chemical Property of 3-Methoxy-4-methylphenol

Chemical Property:

Boiling Point:240.3 °C at 760 mmHg
Flash Point:116.4 °C
PSA：29.46000
Density:1.078 g/cm³
LogP:1.70920
Storage Temp.:2-8°C
XLogP3:2.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:1
Exact Mass:138.068079557
Heavy Atom Count:10
Complexity:103

Purity/Quality:

97% ^*data from raw suppliers

3-Methoxy-4-methylphenol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C=C(C=C1)O)OC

Technology Process of 3-Methoxy-4-methylphenol

There total 6 articles about 3-Methoxy-4-methylphenol 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: 89.0%

: 18278-34-7
4-hydroxy-2-methoxybenzaldehyde

: 19217-50-6
4-methyl-3-(methyloxy)phenol

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In ethanol; acetic acid; at 20 ℃; for 14h; under 3102.97 Torr;

Reference yield:

: 16452-01-0
ortho-cresidine

: 19217-50-6
4-methyl-3-(methyloxy)phenol

Guidance literature:: Multistep reaction; (i) (diazotization), (ii) (hydrolysis);
DOI:10.1021/jm00294a015

Reference yield:

: 13120-77-9
2-methyl-5-nitroanisole

: 19217-50-6
4-methyl-3-(methyloxy)phenol

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / Ni-Raney / methanol / 20 °C / 760.05 Torr

2: water; sodium nitrite; sulfuric acid / 1.5 h / 0 - 90 °C

With sulfuric acid; water; hydrogen; sodium nitrite; Ni-Raney; In methanol;