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2-Hydroxy-4-methoxybenzaldehyde structure, CAS 673-22-3

2-Hydroxy-4-methoxybenzaldehyde

CAS Number673-22-3

Synonymso-Hydroxy-p-methoxybenzaldehyde; VHR BQ DO1; 2-Hydroxy-4-methoxybenzaldehyde; 4-Methoxysalicylaldehyde; 4-Methoxysalicyaldehyde; Benzaldehyde,2-hydroxy-4-methoxy; 2-Hydroxy-p-anisaldehyde; p-Anisaldehyde,2-hydroxy; 2-hydroxy-4-methoxy benzaldehyde; 4-methoxy-salicylaldehyde; Salicylaldehyde,4-methoxy; EINECS 211-604-0; 4-methoxy-2-hydroxybenzaldehyde; MFCD00003327

Molecular FormulaHOC6H3(OCH3)CHO

Molecular Weight152.15

Purity98%

Density1.2±0.1 g/cm3

Boiling Point271.5±20.0 °C at 760 mmHg

Melting Point41-43 °C (lit.)

Flash Point

Appearancecolorless needle crystal

EINECS211-604-0

MSDSChineseEnglish

SymbolTransport

Signal WordWarning

Cat. No.: 2A-9003222 Purity: 98%
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Quality Control of [ 673-22-3 ] Purity: 98% SDS Specification MoL

COA NMR CNMR HPLC LC-MS
Chemical & Physical Properties
CAS Number673-22-3
Catalog No.2A-9003222
Chinese Name2-羟基-4-甲氧基苯甲醛
Synonymso-Hydroxy-p-methoxybenzaldehyde; VHR BQ DO1; 2-Hydroxy-4-methoxybenzaldehyde; 4-Methoxysalicylaldehyde; 4-Methoxysalicyaldehyde; Benzaldehyde,2-hydroxy-4-methoxy; 2-Hydroxy-p-anisaldehyde; p-Anisaldehyde,2-hydroxy; 2-hydroxy-4-methoxy benzaldehyde; 4-methoxy-salicylaldehyde; Salicylaldehyde,4-methoxy; EINECS 211-604-0; 4-methoxy-2-hydroxybenzaldehyde; MFCD00003327
Molecular FormulaHOC6H3(OCH3)CHO
Molecular Weight152.15
Purity98
Density1.2±0.1 g/cm3
Boiling Point271.5±20.0 °C at 760 mmHg
Melting Point41-43 °C (lit.)
Appearancecolorless needle crystal
Storage ConditionStore in an airtight container in a cool, dry plac
Application2-Hydroxy-4-methoxybenzaldehyde is an isomer of vanillin and can be used to synthesize uridine M7. 2-Hydroxy-4-methoxybenzaldehyd is a potent tyrosinase inhibitor derived from three East African medic
EINECS211-604-0
HTC29124900
PubChem ID24849887
MDL NumberMFCD00003327
SMILES[H]C(=O)c1ccc(OC)cc1O
InChI1S/C8H8O3/c1-11-7-3-2-6(5-9)8(10)4-7/h2-5,10H,1H3
InChI KeyWZUODJNEIXSNEU-UHFFFAOYSA-N
Beilstein/REAXYS1072443
NACRES CodeNA.22
UNSPSC12352100
Hazard SymbolsTransport
MSDSmsds/3222_1_673_22_3.pdf
Bioactivity2-Hydroxy-4-methoxybenzaldehyde, a chemical compound and an isomer of Vanillin, could be used to synthesis Urolithin M7[1]. 2-hydroxy-4-methoxybenzaldehyde is a potent tyrosinase inhibitor from three East African medicinal plants, Mondia whitei, Rhus vulgaris Meikle, and Sclerocarya caffra Sond[2]. Related Catalog Research Areas >> Others Signaling Pathways >> Metabolic Enzyme/Protease >> Tyrosinase Target Tyrosinase[2]. References [1]. Bodwell Graham, et al. An Inverse Electron-Demand Diels-Alder-Based Total Synthesis of Urolithin M7. Synlett. 2011 (15): 2245. [2]. Kubo I, et al. 2-Hydroxy-4-methoxybenzaldehyde: a potent tyrosinase inhibitor from African medicinal plants. Planta Med. 1999 Feb;65(1):19-22. Chemical & Physical Properties Density 1.2±0.1 g/cm3 Boiling Point 271.5±20.0 °C at 760 mmHg Melting Point 41-43 °C(lit.) Molecular Formula C8H8O3 Molecular Weight 152.15 Flash Point 112.1±15.3 °C Exact Mass 152.047348 PSA 46.53000 LogP 1.79 Vapour Pressure 0.0±0.6 mmHg at 25°C Index of Refraction 1.588 InChIKey WZUODJNEIXSNEU-UHFFFAOYSA-N SMILES COc1ccc(C=O)c(O)c1
Use of2-Hydroxy-4-methoxybenzaldehyde, a chemical compound and an isomer of Vanillin, could be used to synthesis Urolithin M7[1]. 2-hydroxy-4-methoxybenzaldehyde is a potent tyrosinase inhibitor from three East African medicinal plants, Mondia whitei, Rhus vulgaris Meikle, and Sclerocarya caffra Sond[2]. Properties Articles15 Name 2-Hydroxy-4-methoxybenzaldehyde Synonym More Synonyms 2-Hydroxy-4-methoxybenzaldehyde Biological Activity Description 2-Hydroxy-4-methoxybenzaldehyde, a chemical compound and an isomer of Vanillin, could be used to synthesis Urolithin M7[1]. 2-hydroxy-4-methoxybenzaldehyde is a potent tyrosinase inhibitor from three East African medicinal plants, Mondia whitei, Rhus vulgaris Meikle, and Sclerocarya caffra Sond[2]. Related Catalog Research Areas >> Others Signaling Pathways >> Metabolic Enzyme/Protease >> Tyrosinase Tyrosinase[2]. References [1]. Bodwell Graham, et al. An Inverse Electron-Demand Diels-Alder-Based Total Synthesis of Urolithin M7. Synlett. 2011 (15): 2245. [2]. Kubo I, et al. 2-Hydroxy-4-methoxybenzaldehyde: a potent tyrosinase inhibitor from African medicinal plants. Planta Med. 1999 Feb;65(1):19-22. Chemical & Physical Properties Molecular Formula C8H8O3 Exact Mass 152.047348 PSA 46.53000 Index of Refraction 1.588 InChIKey WZUODJNEIXSNEU-UHFFFAOYSA-N
Tax Rebate9.0%
SupervisionNone. MFN tariff: 5.5%. Ordinary tariff: 30.0%
Transport InfoProduct name: Purity: 98.0%
MSDS Transport InfoModule 14. Shipping information 14.1 UN dangerous goods number European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.2 Names specified by the United Nations (UN) European Land Transport Dangerous Regulations: Non-dangerous goods IMDG Code: Non-dangerous goods International air transport dangerous goods regulations: non-dangerous goods 14.3 Transport hazard categories European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.4 Package group European Land Transport Dangerous Regulations: -International Maritime Dangerous Regulations: -International Air Transport Dangerous Regulations: - 14.5 Environmental hazards European Land Transport Dangerous Regulations: No International Maritime Transport Dangerous Regulations Maritime Pollutants: No International Air Transport Risk Regulations: No 14.6 Special reminder to users No data available
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