4-Methoxy-2,3-dimethylbenzaldehyde

Base Information

• Chemical Name: 4-Methoxy-2,3-dimethylbenzaldehyde
• CAS No.: 38998-17-3
• Molecular Formula: C10H12O2
• Molecular Weight: 164.204
• Hs Code.: 2912499000
• European Community (EC) Number: 254-241-3
• DSSTox Substance ID: DTXSID80192275
• Nikkaji Number: J319.886C
• Wikidata: Q72470842
• Mol file: 38998-17-3.mol

Synonyms:38998-17-3;4-Methoxy-2,3-dimethylbenzaldehyde;2,3-Dimethyl-4-methoxybenzaldehyde;2,3-Dimethylanisaldehyde;Benzaldehyde, 4-methoxy-2,3-dimethyl-;2,3-Dimethyl-p-anisaldehyde;EINECS 254-241-3;4-methoxy-2,3-dimethyl-benzaldehyde;MFCD00003339;Talampicillinhydrochloride;SCHEMBL851964;2,3-Dimethyl-para-anisaldehyde;DTXSID80192275;2,3-dimethyl 4-methoxy benzaldehyde;CL8242;4-Methoxy-2,3-dimethylbenzaldehyde #;AKOS004907347;CS-W017904;AS-10311;2,3-Dimethyl-4-methoxybenzaldehyde, 99%;FT-0639509;EN300-704108;A824370;Z1255485215

Chemical Property of 4-Methoxy-2,3-dimethylbenzaldehyde

Chemical Property:

• Vapor Pressure: 0.00374mmHg at 25°C
• Melting Point: 52-55 °C(lit.)
• Refractive Index: 1.538
• Boiling Point: 280.629 °C at 760 mmHg
• Flash Point: 124.796 °C
• PSA: 26.30000
• Density: 1.042 g/cm³
• LogP: 2.12450
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 164.083729621
• Heavy Atom Count: 12
• Complexity: 156

Purity/Quality:

99% ^*data from raw suppliers

4-Methoxy-2,3-dimethylbenzaldehyde ^*data from reagent suppliers

Safty Information:

• Safety Statements: 22-24/25

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

• Canonical SMILES: CC1=C(C=CC(=C1C)OC)C=O
• Uses: 2,3-Dimethyl-4-methoxybenzaldehyde (2,3-Dimethylanisaldehyde) was used to prepare β-aryl-β-ketophosphonates.

Technology Process of 4-Methoxy-2,3-dimethylbenzaldehyde

There total 3 articles about 4-Methoxy-2,3-dimethylbenzaldehyde 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:

2,3-dimethylanisole (2944-49-2) + N,N-dimethyl-formamide (68-12-2,33513-42-7) → 2,3-dimethyl-4-methoxybenzaldehyde (38998-17-3)

Guidance literature:

With trichlorophosphate;

Reference yield:

2,3-Dimethylphenol (526-75-0) → 2,3-dimethyl-4-methoxybenzaldehyde (38998-17-3)

Guidance literature:

Multi-step reaction with 2 steps

1: K₂CO₃

2: (i) POCl₃, (ii) /BRN= 1859736/

With potassium carbonate;

Reference yield:

→ 2,3-dimethyl-4-methoxybenzaldehyde (38998-17-3)

Guidance literature:

upstream raw materials:

2,3-dimethylanisole

N,N-dimethyl-formamide

2,3-Dimethylphenol

Downstream raw materials:

2,3-Dimethylhydroquinone monomethyl ether

4-Methoxy-2,3-dimethylzimtsaeure

C₃₀H₂₆O₃

2-[(E)-4-(4-Methoxy-2,3-dimethyl-phenyl)-but-3-enyl]-isoindole-1,3-dione