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454664

Sigma-Aldrich

2-Hydroxy-5-methylbenzaldehyde

98%

Synonym(s):

5-Methylsalicylaldehyde, 2,5-Cresotaldehyde

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About This Item

Linear Formula:
HOC6H3(CH3)CHO
CAS Number:
613-84-3
Molecular Weight:
136.15
Beilstein/REAXYS Number:
2040673
EC Number:
210-357-6
MDL number:
MFCD00274297
UNSPSC Code:
12352100
PubChem Substance ID:
24868951
NACRES:
NA.22

assay

98%

form

solid

bp

217 °C (lit.)

mp

54-57 °C (lit.)

functional group

aldehyde

SMILES string

Cc1ccc(O)c(C=O)c1

InChI

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

InChI key

ILEIUTCVWLYZOM-UHFFFAOYSA-N

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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

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBP5405V
BGBB9800
BGBB2925
BGBB2925V
09011HJ

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Berelli Anupama et al.
Journal of fluorescence, 27(3), 953-965 (2017-01-18)
Ternary Cu(II) complexes [Cu(II)(L)(bpy)Cl] 1, [Cu(II)(L)(Phen)Cl] 2 [L = 2,3-dimethyl-1-phenyl-4(2 hydroxy-5-methyl benzylideneamino)-pyrazol-5-one, bpy = 2,2
Spectroscopy and stereochemistry of the optically active copper (II), cobalt (II) and nickel (II) complexes with Schiff bases N,N'-(1R,2R)-(-)-1, 2-cyclohexylenebis(3-methylbenzylideneiminato) and N,N'-(1R,2R)-(-)-1,2-cyclohexylenebis(5-methylbenzylideneiminato)
Szlyk E, et al.
Polyhedron, 21(27), 2711-2717 (2002)
Syntheses, structures and electrochemistry of copper (II) salicylaldehyde/tris (3-phenylpyrazolyl) borate complexes as models for the radical copper oxidases.
Halcrow MA, et al.
J. Chem. Soc., Dalton Trans., 11, 1753-1762 (1999)
Atsuko Masuya-Suzuki et al.
ChemistryOpen, 10(1), 46-55 (2021-01-22)
We prepared Ln(III) (Ln=Eu, Gd, and Yb) complexes with a tripodal Schiff base, tris[2-(5-methylsalicylideneimino)ethyl]amine (H3 L) and studied their photophysical properties. Upon ligand excitation, YbL showed Yb(III)-centered luminescence in the near-infrared region. While the overall quantum yield (0.60(1)%) of YbL
Bijoy Dey et al.
Chemistry, an Asian journal, 15(11), 1709-1721 (2020-04-18)
The reaction of Fe(NCS)3 prepared in situ in MeOH with 5-X-SalEen ligands (5-X-SalEen=condensation product of 5-substituted salicylaldehyde and N-ethylethylenediamine) provided three Fe(III) complexes, [Fe(5-X-SalEen)2 ]NCS; X=Me (1), X=Br (2), X=OMe (3). All the complexes reveal similar structural features but a very
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