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:
Molecular Weight:
136.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
1099377
Assay:
98%
Form:
liquid
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
Quality Level
bp
204 °C/730 mmHg (lit.)
density
1.123 g/mL at 25 °C (lit.)
functional group
aldehyde
Related Categories
signalword
Warning
hcodes
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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Synthesis and characterization of amino acid Schiff base complexes of nickel (II).
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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
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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
8-Substituted 3-Arylcoumarins as Potent and Selective MAO-B Inhibitors: Synthesis, Pharmacological Evaluation, and Docking Studies.
Vi?a D, et al.
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[2-(1H-Benzimidazol-2-yl-?N3) aniline-?N] dichloridozinc.
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