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35431-26-6

35431-26-6 Structure

35431-26-6 Structure
IdentificationBack Directory
[Name]

5-Hydroxy-2-methoxybenzaldehyde
[CAS]

35431-26-6
[Synonyms]

5-Hydroxy-2-methoxybenzaldehyde
2-Methoxy-5-hydroxybenzaldehyde
Benzaldehyde, 5-hydroxy-2-methoxy-
5-Hydroxy-2-methoxybenzaldehyde 95+%
5-Hydroxy-2-methoxybenzaldehyde ISO 9001:2015 REACH
[Molecular Formula]

C8H8O3
[MDL Number]

MFCD03820046
[MOL File]

35431-26-6.mol
[Molecular Weight]

152.15
Chemical PropertiesBack Directory
[Melting point ]

110-115 °C
[Boiling point ]

309.0±22.0 °C(Predicted)
[density ]

1.231±0.06 g/cm3(Predicted)
[storage temp. ]

under inert gas (nitrogen or Argon) at 2-8°C
[solubility ]

Acetone (Slightly), DMSO (Slightly)
[form ]

Solid
[pka]

9.73±0.18(Predicted)
[color ]

Light Brown to Dark Orange
[Stability:]

Air Sensitive
[InChI]

1S/C8H8O3/c1-11-8-3-2-7(10)4-6(8)5-9/h2-5,10H,1H3
[InChIKey]

HWNIBJPEJAWOTR-UHFFFAOYSA-N
[SMILES]

COc1ccc(O)cc1C=O
Questions And AnswerBack Directory
[Uses]

5-Hydroxy-2-methoxy-benzaldehyde is a phenolic substance that can be used in organic synthesis.
Safety DataBack Directory
[Symbol(GHS) ]

Exclamation Mark (GHS07)
GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H319-H335
[Precautionary statements ]

P271-P261
[Hazard Codes ]

Xi
[WGK Germany ]

WGK 3
[HazardClass ]

IRRITANT, AIR SENSITIVE
[HS Code ]

2916399090
[Storage Class]

11 - Combustible Solids
[Hazard Classifications]

Acute Tox. 4 Oral
Aquatic Chronic 3
Eye Irrit. 2
Skin Sens. 1
Hazard InformationBack Directory
[Synthesis Reference(s)]

The Journal of Organic Chemistry, 39, p. 2437, 1974 DOI: 10.1021/jo00930a032
[Synthesis]

Benzaldehyde, 2-methoxy-5-(methoxymethoxy)-

142677-24-5

5-Hydroxy-2-methoxybenzaldehyde

35431-26-6

The general procedure for the synthesis of 5-hydroxy-2-methoxybenzaldehyde from 2-methoxy-5-(methoxymethoxy)benzaldehyde was as follows: to a solution of 2-methoxy-5-(methoxymethoxy)benzaldehyde (33.5 g, 0.17 mol, 1 eq.) in tetrahydrofuran (THF, 150 mL) was added 3N hydrochloric acid (HCl, 250 mL, 4.4 eq.). The reaction mixture was stirred at 50 °C for 1 h, subsequently cooled to room temperature and diluted with deionized water (500 mL). The mixture was neutralized to pH 7-8 with solid potassium carbonate (K2CO3). the light yellow solid product was collected by filtration, washed with deionized water and dried to afford 5-hydroxy-2-methoxybenzaldehyde (17.9 g, 74.6% yield) as a light yellow solid. The product was confirmed by NMR hydrogen spectrum (400 MHz, DMSO-d6): δ= 10.31 (s, 1H), 8.03 (s, 1H), 6.89 (s, 1H), 3.80 (s, 3H). Low resolution mass spectrometry (LRMS) showed the molecular ion peak (M+H+) m/z 154.0.

[References]

[1] Patent: WO2013/102142, 2013, A1. Location in patent: Paragraph 0193
[2] Patent: WO2013/102142, 2013, A1. Location in patent: Paragraph 0172
Spectrum DetailBack Directory
[Spectrum Detail]

5-Hydroxy-2-methoxybenzaldehyde(35431-26-6)1HNMR
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