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392936

2,6-Dimethoxy-4-hydroxybenzaldehyde

Name: 2,6-Dimethoxy-4-hydroxybenzaldehyde
Brand: ALDRICH

95%

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About This Item

Linear Formula:

HOC₆H₂(OCH₃)₂CHO

CAS Number:

22080-96-2

Molecular Weight:

182.17

NACRES:

NA.22

PubChem Substance ID:

24864151

UNSPSC Code:

12352100

MDL number:

MFCD01407645

Assay:

95%

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Properties

assay

95%

mp

225 °C (dec.) (lit.)

functional group

aldehyde

SMILES string

COc1cc(O)cc(OC)c1C=O

InChI

1S/C9H10O4/c1-12-8-3-6(11)4-9(13-2)7(8)5-10/h3-5,11H,1-2H3

InChI key

HZWPJAZIRZFCGX-UHFFFAOYSA-N

Description

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.

Application

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.

pictograms

GHS07

signalword

Warning

hcodes

H315,H319,H335

pcodes

P261 - P264 - P271 - P280 - P302 + P352 - P305 + P351 + P338

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

Regulatory Information

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4-Hydroxy-2, 6-dimethoxybenzaldehyde.

Wuyts C, et al.

Acta Crystallographica Section E, Structure Reports Online, 61(1), 79-80 (2004)

Liquid-phase combinatorial synthesis of 1,4-benzodiazepine-2,5-diones as the candidates of endothelin receptor antagonism.

Ming-Fu Cheng et al.

Journal of combinatorial chemistry, 6(1), 99-104 (2004-01-13)

A library of 1,4-benzodiazepine-2,5-dione dicarboxylate derivatives containing aryl substituents at N(1)- and N(4)-positions to mimic the amino acid residues of Try-13, Phe-14, and Asp-18 in endothelin-1 is established by using the starting materials of alpha-amino esters, hydroxybenzaldehydes, nitrobenzoyl chlorides, and

Antibacterial activities of phenolic benzaldehydes and benzoic acids against Campylobacter jejuni, Escherichia coli, Listeria monocytogenes, and Salmonella enterica.

Mendel Friedman et al.

Journal of food protection, 66(10), 1811-1821 (2003-10-24)

We evaluated the bactericidal activities of 35 benzaldehydes, 34 benzoic acids, and 1 benzoic acid methyl ester against Campylobacter jejuni, Escherichia coli O157:H7, Listeria monocytogenes, and Salmonella enterica when these compounds were substituted on the benzene ring with 0, 1

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Global Trade Item Number

SKU	GTIN
392936-1G	04061825584959