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4,6-Dihydroxy-2-methoxy-3-methylbenzaldehyde

Base Information
  • Chemical Name:4,6-Dihydroxy-2-methoxy-3-methylbenzaldehyde
  • CAS No.:118093-05-3
  • Molecular Formula:C9H10O4
  • Molecular Weight:182.176
  • Hs Code.:
  • DSSTox Substance ID:DTXSID50699049
  • Wikidata:Q82629730
  • Mol file:118093-05-3.mol
4,6-Dihydroxy-2-methoxy-3-methylbenzaldehyde

Synonyms:4,6-dihydroxy-2-methoxy-3-methylbenzaldehyde;118093-05-3;4,6-DIHYDROXY-2-METHOXY-3-METHYL BENZALDEHYDE;DTXSID50699049

Suppliers and Price of 4,6-Dihydroxy-2-methoxy-3-methylbenzaldehyde
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Total 1 raw suppliers
Chemical Property of 4,6-Dihydroxy-2-methoxy-3-methylbenzaldehyde
Chemical Property:
  • PSA:66.76000 
  • LogP:1.22730 
  • XLogP3:1.6
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:2
  • Exact Mass:182.05790880
  • Heavy Atom Count:13
  • Complexity:183
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CC1=C(C(=C(C=C1O)O)C=O)OC
Technology Process of 4,6-Dihydroxy-2-methoxy-3-methylbenzaldehyde

There total 11 articles about 4,6-Dihydroxy-2-methoxy-3-methylbenzaldehyde 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:
Guidance literature:
With lithium hydroxide; In water; at 90 ℃; for 4h;
DOI:10.1002/anie.201705390
Guidance literature:
With palladium on activated charcoal; hydrogen; In methanol; ethyl acetate; at 20 ℃; for 12h; under 760.051 - 3800.26 Torr;
Guidance literature:
Multi-step reaction with 7 steps
1.1: trichlorophosphate / 1 h / 0 °C
2.1: hydrazine hydrate / ethylene glycol / 3 h / 80 °C
2.2: 3 h / 120 °C
3.1: trichlorophosphate / 0 °C
4.1: boron tribromide / dichloromethane / -78 - 20 °C / Inert atmosphere
5.1: potassium carbonate / acetone / 60 °C / Cooling with ice
6.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / N,N-dimethyl-formamide / 60 °C / Cooling with ice
7.1: palladium on activated charcoal; hydrogen / ethyl acetate; methanol / 12 h / 20 °C / 760.05 - 3800.26 Torr
With palladium on activated charcoal; hydrogen; boron tribromide; potassium carbonate; hydrazine hydrate; 1,8-diazabicyclo[5.4.0]undec-7-ene; trichlorophosphate; In methanol; dichloromethane; ethylene glycol; ethyl acetate; N,N-dimethyl-formamide; acetone;
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