2,3-Dimethoxybenzaldehyde

2,3-Dimethoxybenzaldehyde
  • CAS No.:86-51-1
Other grades of this product :
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;Aromatic Aldehydes & Derivatives (substituted);BenzaldehydeDerivative;Benzaldehyde;Building Blocks;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks
Mol File:86-51-1.mol
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)
Fp >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
InChIKeyJIVGSHFYXPRRSZ-UHFFFAOYSA-N
CAS DataBase Reference86-51-1(CAS DataBase Reference)
NIST Chemistry ReferenceBenzaldehyde, 2,3-dimethoxy-(86-51-1)
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 Information
ProviderLanguage
2,3-Dimethoxybenzaldehyde English
SigmaAldrich English
ACROS English
ALFA English
2,3-Dimethoxybenzaldehyde Usage And Synthesis
Chemical Propertieswhite to brown crystalline powder
UsesA 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.
Uses2,3-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.
Safety ProfileA poison by ingestion. When heated to decomposition it emits acrid smoke and irritating vapors

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