516325
4-Methoxy-2-methylbenzaldehyde
95%
Synonym(s):
2-Methyl-p-anisaldehyde
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About This Item
Linear Formula:
CH3C6H3(OCH3)CHO
CAS Number:
Molecular Weight:
150.17
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
95%
refractive index
n20/D 1.571 (lit.)
bp
262-267 °C (lit.)
density
1.107 g/mL at 25 °C (lit.)
SMILES string
[H]C(=O)c1ccc(OC)cc1C
InChI
1S/C9H10O2/c1-7-5-9(11-2)4-3-8(7)6-10/h3-6H,1-2H3
InChI key
WICYVKGMEJSDAO-UHFFFAOYSA-N
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves
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Compounds of potential interest for the chemotherapy of leprosy.
Buu-Hoi NP, et al.
The Journal of Organic Chemistry, 21(4), 415-418 (1956)
Tamer Awad et al.
Journal of chromatographic science, 45(8), 458-465 (2007-11-21)
The methoxy methyl phenylacetones share an isobaric relationship (equivalent mass but different elemental composition) to the controlled precursor substance 3,4-methylenedioxyphenylacetone. The 10 methoxy methyl phenylacetones as well as the methylenedioxyphenylacetones show essentially equivalent mass spectra with major fragment ions at
Estrogenic Biphenyls. III. 2-Alkyl-4-methoxybiphenyl-4'-carboxylic Acids.
Sato T and Oki M.
Bulletin of the Chemical Society of Japan, 30(8), 859-862 (1957)
Jong H Kim et al.
Annals of clinical microbiology and antimicrobials, 10, 23-23 (2011-06-02)
Disruption of cellular antioxidation systems should be an effective method for control of fungal pathogens. Such disruption can be achieved with redox-active compounds. Natural phenolic compounds can serve as potent redox cyclers that inhibit microbial growth through destabilization of cellular
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