2,4-Dichloro-5-methylbenzene-1,3-diol

Base Information

Chemical Name:2,4-Dichloro-5-methylbenzene-1,3-diol
CAS No.:88207-72-1
Molecular Formula:C7H6Cl2O2
Molecular Weight:193.029
Hs Code.:
DSSTox Substance ID:DTXSID80565485
Nikkaji Number:J801.918E
Wikidata:Q82450606

Synonyms:2,4-Dichloro-5-methylbenzene-1,3-diol;88207-72-1;SCHEMBL67759;DTXSID80565485

Suppliers and Price of 2,4-Dichloro-5-methylbenzene-1,3-diol

Supply Marketing:

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

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Chemical Property of 2,4-Dichloro-5-methylbenzene-1,3-diol

Chemical Property:

XLogP3:2.8
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:191.9744848
Heavy Atom Count:11
Complexity:142

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=CC(=C(C(=C1Cl)O)Cl)O

Technology Process of 2,4-Dichloro-5-methylbenzene-1,3-diol

There total 2 articles about 2,4-Dichloro-5-methylbenzene-1,3-diol 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:

: 2524-37-0
ethyl orselinate

: 88207-72-1
2,4-dichloro-5-methyl-resorcinol

Guidance literature:: Multi-step reaction with 2 steps

1: tetrachloromethane; chlorine

2: aqueous KOH

With tetrachloromethane; potassium hydroxide; chlorine;

Reference yield:

: 27808-83-9
ethyl 3,5-dichloro-2,4-dihydroxy-6-methylbenzoate

: 88207-72-1
2,4-dichloro-5-methyl-resorcinol

Guidance literature:: With potassium hydroxide;

Reference yield:

: 88207-72-1
2,4-dichloro-5-methyl-resorcinol

: 88207-75-4
2,3,5,6-tetraacetoxy-4-chloro-toluene

Guidance literature:: Multi-step reaction with 3 steps

1: Fremy's salt, K₂HPO₄ / H₂O / 24 h / Ambient temperature

2: 39 percent / NaOH / H₂O / 2 h / Heating

3: 1.) H₂, 2.) NaOAc / 1.) 10percent Pd-carbon / 1.) ethyl acetate, 1 h, 2.) 100 deg C, 15 min

With sodium hydroxide; dipotassium hydrogenphosphate; potassiuim nitrosodisulfonate; hydrogen; sodium acetate; palladium on activated charcoal; In water;