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Merck
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文件

516325

Sigma-Aldrich

4-甲氧基-2-甲基苯甲醛

95%

别名:

2-甲基-对茴香醛

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About This Item

线性分子式:
CH3C6H3(OCH3)CHO
CAS号:
52289-54-0
分子量:
150.17
MDL號碼:
MFCD02261771
分類程式碼代碼:
12352100
PubChem物質ID:
24873879
NACRES:
NA.22

化驗

95%

折射率

n20/D 1.571 (lit.)

bp

262-267 °C (lit.)

密度

1.107 g/mL at 25 °C (lit.)

SMILES 字串

[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 密鑰

WICYVKGMEJSDAO-UHFFFAOYSA-N

儲存類別代碼

12 - Non Combustible Liquids

水污染物質分類（WGK）

WGK 3

閃點（°F）

Not applicable

閃點（°C）

Not applicable

個人防護裝備

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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