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Merck
CN

444553

2-Hydroxy-3-methylbenzaldehyde

98%

Synonym(s):

3-Methylsalicylaldehyde, 2,3-Cresotaldehyde, 2-Hydroxy-3-methylbenzaldehyde

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About This Item

Linear Formula:
HOC6H3(CH3)CHO
CAS Number:
824-42-0
Molecular Weight:
136.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
24868130
MDL number:
MFCD00040798
Beilstein/REAXYS Number:
1099377

Key Documents

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Product Name

2-Hydroxy-3-methylbenzaldehyde, 98%

InChI

1S/C8H8O2/c1-6-3-2-4-7(5-9)8(6)10/h2-5,10H,1H3

SMILES string

Cc1cccc(C=O)c1O

InChI key

IPPQNXSAJZOTJZ-UHFFFAOYSA-N

assay

98%

form

liquid

refractive index

n20/D 1.564 (lit.)

bp

204 °C/730 mmHg (lit.)

density

1.123 g/mL at 25 °C (lit.)

functional group

aldehyde

Quality Level

100

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pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

188.6 °F - closed cup

flash_point_c

87 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

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Certificates of Analysis (COA)

Lot/Batch Number
MKCB1819V
MKBL4111V
MKBG0916V
MKBB1762
03221PH

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8-Substituted 3-Arylcoumarins as Potent and Selective MAO-B Inhibitors: Synthesis, Pharmacological Evaluation, and Docking Studies.
Vi?a D, et al.
ChemMedChem, 7(3), 464-470 (2012)
Irina A Kühne et al.
Journal of physics. Condensed matter : an Institute of Physics journal, 32(40), 404002-404002 (2020-03-26)
Structural, magnetic and electromechanical changes resulting from spin crossover between the spin quintet and spin triplet forms of a mononuclear Mn3+ complex embedded in six lattices with different charge balancing counterions are reported. Isostructural ClO4- and BF4- salts (1) and
[2-(1H-Benzimidazol-2-yl-?N3) aniline-?N] dichloridozinc.
Eltayeb NE, et al.
Acta Crystallographica Section E, Structure Reports Online, 67(8), 1062-1063 (2011)
P Valenti et al.
Bioorganic & medicinal chemistry, 6(6), 803-810 (1998-07-29)
A series of 1,4-dihydropyridines bearing a coumarin moiety in 4-position was synthesized. The compounds were evaluated for inotropic, chronotropic and calcium antagonist activities. The replacement of the o-nitrophenyl moiety of nifedipine with a coumarin or phenylcoumarin system is accompanied by
Synthesis and characterization of amino acid Schiff base complexes of nickel (II).
Wang G and Chang JC.
Synth. React. Inorg. Met.-Org. Chem. , 24(7), 1091-1097 (1994)

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