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2,3-Dimethoxybenzaldehyde

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2,3-Dimethoxybenzaldehyde Basic information

Product Name:
2,3-Dimethoxybenzaldehyde
Synonyms:
  • 3,5-Dihydroxypropiophenone
  • 3,5-Dimethylsalicylic acid
  • LABOTEST-BB LT00932325
  • BENZALDEHYDE, 2,3-DIMETHOXY-
  • O-VERATRALDEHYDE
  • O-VERATRIC ALDEHYDE
  • 4-Diethoxybenzene
  • 2,3-Dimethoxybenzenecarbonal
CAS:
86-51-1
MF:
C9H10O3
MW:
166.17
EINECS:
201-677-7
Product Categories:
  • Inhibitors
  • Aldehydes
  • C9
  • Carbonyl Compounds
  • Aromatics
  • Miscellaneous Reagents
  • Building Blocks
  • Carbonyl Compounds
  • Chemical Synthesis
  • Organic Building Blocks
  • BenzaldehydeDerivative
  • Benzaldehyde
  • Aromatic Aldehydes & Derivatives (substituted)
Mol File:
86-51-1.mol
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2,3-Dimethoxybenzaldehyde Chemical Properties

Melting point:
48-52 °C (lit.)
Boiling point:
137 °C/12 mmHg (lit.)
Density 
1.1708 (rough estimate)
refractive index 
1.5500 (estimate)
Flash point:
>230 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
solubility 
Solubility in methanol with almost transparency.
form 
Crystalline Powder, Crystals, and/or Chunks
color 
Off-white to beige
Sensitive 
Air Sensitive
BRN 
908264
InChIKey
JIVGSHFYXPRRSZ-UHFFFAOYSA-N
LogP
1.630 (est)
CAS DataBase Reference
86-51-1(CAS DataBase Reference)
NIST Chemistry Reference
Benzaldehyde, 2,3-dimethoxy-(86-51-1)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
RTECS 
CU5732000
Hazard Note 
Irritant
HS Code 
29124900

MSDS

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2,3-Dimethoxybenzaldehyde Usage And Synthesis

Description

2,3-Dimethoxybenzaldehyde, commonly known as o-veratrol, is an important aromatic aldehyde compound. Its structure is characterized by two methoxy substituents and one aldehyde group at the ortho (2 and 3) positions of the benzene ring. Due to its unique chemical structure, this compound occupies a central position in the field of pharmaceutical intermediates, especially as a key precursor in the synthesis of berberine. Furthermore, it possesses significant biological activities, such as antifungal and antiviral effects.

Chemical Properties

white to brown crystalline powder

Uses

2,3-Dimethoxybenzaldehyde possess antifungal activity of redox-active benzaldehydes that target cellular antioxidation. It could function as chemosensitizing agents in concert with conventional drugs to improve antifungal efficacy.

Uses

A benzaldehyde derivative that may possess antifungal activity of redox-active benzaldehydes that target cellular antioxidation. It could function as chemosensitizing agents in concert with convention al drugs or fungicides to improve antifungal efficacy.

Safety Profile

A poison by ingestion. When heated to decomposition it emits acrid smoke and irritating vapors

2,3-Dimethoxybenzaldehyde Preparation Products And Raw materials

Raw materials

Preparation Products

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