2-Hydroxy-3-methoxy-5-methylbenzoic acid

Base Information

Chemical Name:2-Hydroxy-3-methoxy-5-methylbenzoic acid
CAS No.:4386-42-9
Molecular Formula:C9H10O4
Molecular Weight:182.176
Hs Code.:2918990090
NSC Number:109122
DSSTox Substance ID:DTXSID40296400
Nikkaji Number:J2.751.047G
Wikidata:Q82036992
Mol file:4386-42-9.mol

Synonyms:2-hydroxy-3-methoxy-5-methylbenzoic acid;4386-42-9;NSC109122;SCHEMBL14363157;DTXSID40296400;AKOS008119598;NSC-109122;2-hydroxy-3-methoxy-5-methylbenzoicacid;CS-0452524;EN300-71665;Z367679332

Suppliers and Price of 2-Hydroxy-3-methoxy-5-methylbenzoic acid

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-hydroxy-3-methoxy-5-methylbenzoicacid
250mg
$ 310.00

TRC
2-hydroxy-3-methoxy-5-methylbenzoicacid
25mg
$ 45.00

Crysdot
2-Hydroxy-3-methoxy-5-methylbenzoicacid 95+%
1g
$ 313.00

Alichem
2-Hydroxy-3-methoxy-5-methylbenzoicacid
1g
$ 400.00

AK Scientific
2-Hydroxy-3-methoxy-5-methylbenzoicacid
10g
$ 1836.00

AK Scientific
2-Hydroxy-3-methoxy-5-methylbenzoicacid
1g
$ 503.00

Total 9 raw suppliers

Chemical Property of 2-Hydroxy-3-methoxy-5-methylbenzoic acid

Chemical Property:

Vapor Pressure:6.92E-05mmHg at 25°C
Boiling Point:329.9°Cat760mmHg
Flash Point:133.8°C
PSA：66.76000
Density:1.295g/cm³
LogP:1.40740
XLogP3:2.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:182.05790880
Heavy Atom Count:13
Complexity:192

Purity/Quality:

97% ^*data from raw suppliers

2-hydroxy-3-methoxy-5-methylbenzoicacid ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 2-Hydroxy-3-methoxy-5-methylbenzoic acid

There total 6 articles about 2-Hydroxy-3-methoxy-5-methylbenzoic acid 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: 98.0%

: 93-51-6
2-Methoxy-4-methylphenol

: 124-38-9,18923-20-1
carbon dioxide

: 4386-42-9
2-hydroxy-3-methoxy-5-methylbenzoic acid

Guidance literature:: 2-Methoxy-4-methylphenol; carbon dioxide; With potassium carbonate; at 200 ℃; for 4.5h; under 41372.9 Torr; Autoclave;

With hydrogenchloride; In water; at 20 ℃; pH=1;
DOI:10.1021/jo900922q

Reference yield:

: 13990-86-8
3,3'-dimethoxy-5,5'-dimethyl-[1,1'-biphenyl]-2,2'-diol

: 498-23-7,7407-59-2
citraconic acid

: 498-21-5,636-60-2
2-methylbutanedioic acid

: 7452-10-0
2-hydroxy-3-methoxy-5-methylbenzaldehyde

: 4386-42-9
2-hydroxy-3-methoxy-5-methylbenzoic acid

Guidance literature:: With sodium hydroxide; dihydrogen peroxide; iron(III); at 80 ℃; for 2h; Further Variations:; other metal ions; also without metal ion; Product distribution;
DOI:10.1139/v99-036

Reference yield:

: 93-51-6
2-Methoxy-4-methylphenol

: 298-14-6
potassium hydrogencarbonate

: 4386-42-9
2-hydroxy-3-methoxy-5-methylbenzoic acid

Guidance literature:: With 2,3-dihydroxybenzoate decarboxylase from Aspergillus oryzae; In aq. phosphate buffer; dimethyl sulfoxide; at 30 ℃; for 24h; pH=8.5; Reagent/catalyst; Enzymatic reaction;
DOI:10.1016/j.tetlet.2018.09.019