ChemicalBook Product Catalog Chemical Reagents Organic reagents Aromatic aldehydes 2-Hydroxy-5-methoxybenzaldehyde

2-Hydroxy-5-methoxybenzaldehyde

2-Hydroxy-5-methoxybenzaldehyde Basic information
Product Name:2-Hydroxy-5-methoxybenzaldehyde
Synonyms:2-Formyl-4-methoxyphenol;6-Hydroxy-m-anisaldehyde 5-Methoxysalicylaldehyde;Hydroxy-5-Methoxybenzaldeh;Benzaldehyde,2-hydroxy-5-Methoxy-;2-Hydroxy-5-Methoxybenzaldehyde, 97.5%;2-hydroxy-5-methoxy-benzaldehyd;6-hydroxy-m-anisaldehyd;m-Anisaldehyde, 6-hydroxy-
CAS:672-13-9
MF:C8H8O3
MW:152.15
EINECS:211-589-0
Product Categories:Aromatic Aldehydes & Derivatives (substituted);Benzaldehyde;Adehydes, Acetals & Ketones;Anisoles, Alkyloxy Compounds & Phenylacetates;Phenols
Mol File:672-13-9.mol
2-Hydroxy-5-methoxybenzaldehyde Structure
2-Hydroxy-5-methoxybenzaldehyde Chemical Properties
Melting point 4 °C (lit.)
Boiling point 103 °C/2.5 mmHg (lit.)
density 1.219 g/mL at 25 °C (lit.)
refractive index n20/D 1.578(lit.)
Fp >230 °F
storage temp. Store below +30°C.
form Liquid
pka8.66±0.18(Predicted)
color Clear yellow
Water Solubility Miscible with chloroform. Slightly miscible with water.
Sensitive Air Sensitive
BRN 1100532
InChIKeyFZHSPPYCNDYIKD-UHFFFAOYSA-N
LogP1.520 (est)
CAS DataBase Reference672-13-9(CAS DataBase Reference)
NIST Chemistry ReferenceBenzaldehyde, 2-hydroxy-5-methoxy-(672-13-9)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-36-24/25
WGK Germany 3
RTECS BZ2800000
F 10-23
HS Code 29124900
MSDS Information
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2-Hydroxy-5-methoxybenzaldehyde English
SigmaAldrich English
ACROS English
ALFA English
2-Hydroxy-5-methoxybenzaldehyde Usage And Synthesis
Chemical Propertiesclear yellow liquid
Uses2-Hydroxy-5-methoxybenzaldehyde was used to synthesize radiolabeling precursor desmethyl-PBR06. It was used to study electroantennogram response of the vine weevil (Otiorhynchus sulcatus F.) to a broad range of volatile plant compounds. It was used in the synthesis of tetradentate Schiff base compounds.
Uses2-Hydroxy-5-methoxybenzaldehyde is employed to study electroantennogram response of the vine weevil (Otiorhynchus sulcatus F) to a broad range of volatile plant compounds. It plays an important role in the preparation of tetradentate Schiff base compounds. Further, it is used in the preparation 6-methoxy-3-nitro-2H-chromene by using dibutylamine as a reagent.
DefinitionChEBI: 5-methoxysalicylaldehyde is a member of the class of benzaldehydes carrying hydroxy and methoxy substituents at positions 2 and 5 respectively. It is a member of benzaldehydes, a monomethoxybenzene and a member of phenols. It is functionally related to a salicylaldehyde.
General Description2-Hydroxy-5-methoxybenzaldehyde has acaricidal activity against Tyrophagus putrescentiae.
2,5-DIMETHOXYBENZOYL CHLORIDE 5-Methoxysalicylic acid 2-BROMO-2',5'-DIMETHOXYACETOPHENONE 3-CHLORO-4-HYDROXY-5-METHOXYBENZALDEHYDE OXIME 2-ALLYL-3-HYDROXY-4-METHOXYBENZALDEHYDE 3-FLUORO-4-HYDROXY-5-METHOXYBENZALDEHYDE 2-HYDROXY-5-METHOXY-3-NITRO-BENZALDEHYDE DIHYDROXY BENZALDEHYDE FUMARPROTOCETRARIC ACID 6-BROMO-2-HYDROXY-3-METHOXYBENZALDEHYDE 2-HYDROXY-5-METHOXYBENZOIC ACID SODIUM 2,5-Dimethoxybenzaldehyde 4-HYDROXY-3-METHOXYBENZALDEHYDE (1,3,7-TRIMETHYL-2,6-DIOXO-2,3,6,7-TETRAHYDRO-1H-PURIN-8-YL)HYDRAZONE Glycitein 5-BROMO-2-HYDROXY-3-METHOXYBENZALDEHYDE OXIME 2-Bromo-5-methoxybenzaldehyde 6,7-DIMETHOXY-2,2-DIMETHYL-4-CHLOROMANONE CHLOROPHOSPHONAZO III
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