ChemicalBook--->CAS DataBase List--->22080-96-2

22080-96-2

22080-96-2 Structure

22080-96-2 Structure
IdentificationMore
[Name]

4-Hydroxy-2,6-dimethoxybenzaldehyde
[CAS]

22080-96-2
[Synonyms]

2,6-DIMETHOXY-4-HYDROXYBENZALDEHYDE
3,5-DIMETHOXY-4-FORMYL-PHENOL
4-FORMYL-3,5-DIMETHOXYPHENOL
4-HYDROXY-2,6-DIMETHOXYBENZALDEHYDE
TIMTEC-BB SBB008640
[EINECS(EC#)]

200-110-4
[Molecular Formula]

C9H10O4
[MDL Number]

MFCD01407645
[Molecular Weight]

182.17
[MOL File]

22080-96-2.mol
Chemical PropertiesBack Directory
[Melting point ]

225 °C (dec.)(lit.)
[Boiling point ]

370.4±37.0 °C(Predicted)
[density ]

1.234±0.06 g/cm3(Predicted)
[storage temp. ]

Keep Cold
[pka]

7.04±0.23(Predicted)
[CAS DataBase Reference]

22080-96-2(CAS DataBase Reference)
Safety DataBack Directory
[Hazard Codes ]

Xi
[Risk Statements ]

R36/37/38:Irritating to eyes, respiratory system and skin .
[Safety Statements ]

S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing .
S37/39:Wear suitable gloves and eye/face protection .
[WGK Germany ]

3
[Hazard Note ]

Irritant/Keep Cold
[HS Code ]

29125000
Raw materials And Preparation ProductsBack Directory
[Raw materials]

Ethyl acetate-->PETROLEUM ETHER-->Chloroform-->Potassium hydroxide-->3,5-Dimethoxyphenol-->Silane, (3,5-dimethoxyphenoxy)tris(1-methylethyl)--->Phloroglucinol-->FORMANILIDE
[Preparation Products]

1-(6-hydroxy-2,4-dimethoxy-3-methylphenyl)ethanone-->4,6-DIMETHOXYSALICYLALDEHYDE
Hazard InformationBack Directory
[Chemical Properties]

light yellow powder
[Uses]

2,6-Dimethoxy-4-hydroxybenzaldehyde (4-hydroxy-2,6-dimethoxybenzaldehyde) may be used as a test compound to investigate the bactericidal activity of benzaldehydes against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes and Salmonella enterica.
[Synthesis Reference(s)]

Synthetic Communications, 21, p. 167, 1991 DOI: 10.1080/00397919108020808
[General Description]

2,6-Dimethoxy-4-hydroxybenzaldehyde (4-hydroxy-2,6-dimethoxybenzaldehyde) is a p-hydroxybenzaldehyde derivative. Its synthesis by Vielsmeyer-Haack reaction and confirmation of the product formation by 1H NMR has been reported. Its structure has been investigated. The sodium salt of 4-hydroxy-2,6-dimethoxybenzaldehyde may be used to derivatize Merrifield resin to form resin-bound aldehyde.
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