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516325

Sigma-Aldrich

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:
52289-54-0
Molecular Weight:
150.17
MDL number:
MFCD02261771
UNSPSC Code:
12352100
PubChem Substance ID:
24873879
NACRES:
NA.22

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 Code

12 - Non Combustible Liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBG0955V
10930DH
07318ME
05928HE
07822KD

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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)
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
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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