2,4-Dimethoxy-3-methylbenzyl alcohol

Base Information

Chemical Name:2,4-Dimethoxy-3-methylbenzyl alcohol
CAS No.:78647-61-7
Molecular Formula:C10H14 O3
Molecular Weight:182.22128
Hs Code.:
DSSTox Substance ID:DTXSID50400132
Nikkaji Number:J364.632G
Wikidata:Q82202968
Mol file:78647-61-7.mol

Synonyms:2,4-Dimethoxy-3-methylbenzyl alcohol;(2,4-dimethoxy-3-methylphenyl)methanol;78647-61-7;SCHEMBL697386;DTXSID50400132;AKOS000348551;CS-0280090;EN300-25098226;InChI=1/C10H14O3/c1-7-9(12-2)5-4-8(6-11)10(7)13-3/h4-5,11H,6H2,1-3H

Suppliers and Price of 2,4-Dimethoxy-3-methylbenzyl alcohol

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
2,4-Dimethoxy-3-methylbenzylAlcohol
2.5mg
$ 45.00

Biosynth Carbosynth
2,4-Dimethoxy-3-methylbenzyl alcohol
250 mg
$ 320.00

Biosynth Carbosynth
2,4-Dimethoxy-3-methylbenzyl alcohol
100 mg
$ 170.00

Biosynth Carbosynth
2,4-Dimethoxy-3-methylbenzyl alcohol
50 mg
$ 90.00

Biosynth Carbosynth
2,4-Dimethoxy-3-methylbenzyl alcohol
25 mg
$ 50.00

Total 4 raw suppliers

Chemical Property of 2,4-Dimethoxy-3-methylbenzyl alcohol

Chemical Property:

Vapor Pressure:0.00206mmHg at 25°C
Refractive Index:1.519
Boiling Point:278.3°C at 760 mmHg
Flash Point:128.9°C
PSA：38.69000
Density:1.131 g/mL at 25 °C(lit.)
LogP:1.50450
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:182.094294304
Heavy Atom Count:13
Complexity:149

Purity/Quality:

99% ^*data from raw suppliers

2,4-Dimethoxy-3-methylbenzylAlcohol ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C=CC(=C1OC)CO)OC

Technology Process of 2,4-Dimethoxy-3-methylbenzyl alcohol

There total 3 articles about 2,4-Dimethoxy-3-methylbenzyl alcohol 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: 78.0%

: 7149-92-0
2,4-dimethoxy-3-methylbenzaldehyde

: 78647-61-7
2,4-dimethoxy-3-methylbenzyl alcohol

Guidance literature:: With lithium aluminium tetrahydride; In diethyl ether; for 3h; Ambient temperature;
DOI:10.1039/P19810001685

Reference yield:

: 608-25-3
2-methylbenzene-1,3-diol

: 78647-61-7
2,4-dimethoxy-3-methylbenzyl alcohol

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) hydrogen chloride gas, 2.) water / 1.) ether, 45 min, 2.) 40 deg C

2: 92 percent / potassium carbonate / acetone / 5 h / Heating

3: 78 percent / lithium aluminium hydride / diethyl ether / 3 h / Ambient temperature

With hydrogenchloride; lithium aluminium tetrahydride; water; potassium carbonate; In diethyl ether; acetone;
DOI:10.1039/P19810001685

Reference yield:

: 6248-20-0
2,4-dihydroxy-3-methylbenzaldehyde

: 78647-61-7
2,4-dimethoxy-3-methylbenzyl alcohol

Guidance literature:: Multi-step reaction with 2 steps

1: 92 percent / potassium carbonate / acetone / 5 h / Heating

2: 78 percent / lithium aluminium hydride / diethyl ether / 3 h / Ambient temperature

With lithium aluminium tetrahydride; potassium carbonate; In diethyl ether; acetone;
DOI:10.1039/P19810001685