2-[(2H3)Methyloxy]benzaldehyde

Names

[ CAS No. ]:
56248-49-8

[ Name ]:
2-[(2H3)Methyloxy]benzaldehyde

[Synonym ]:
2-Methoxybenzaldehyde-d3
Benzaldehyde, 2-(methyl-d-oxy)-
2-trideuteriomethoxy-benzaldehyde
o-Methoxy-benzaldehyd
2-[(H)Methyloxy]benzaldehyde
N-sulfonyl 2-aminobenzaldehyde
o-tosylaminobenzaldehyde
o-Trideuteromethoxybenzaldehyd

Biological Activity

[Description]:

2-Methoxybenzaldehyde-d3 is the deuterium labeled 2-Methoxybenzaldehyde[1]. 2-Methoxybenzaldehyde (o-Anisaldehyde), isolated from cinnamon essential oil (CEO), exists antibacterial and antifungal activity[2].

[Related Catalog]:

Research Areas >> Infection
Signaling Pathways >> Anti-infection >> Fungal
Signaling Pathways >> Anti-infection >> Bacterial

[In Vitro]

Stable heavy isotopes of hydrogen, carbon, and other elements have been incorporated into drug molecules, largely as tracers for quantitation during the drug development process. Deuteration has gained attention because of its potential to affect the pharmacokinetic and metabolic profiles of drugs[1].

[References]

[1]. Russak EM, et al. Impact of Deuterium Substitution on the Pharmacokinetics of Pharmaceuticals. Ann Pharmacother. 2019 Feb;53(2):211-216.  

[2]. Zhaoxiang Huang, et al. Synergistic effects of cinnamaldehyde and cinnamic acid in cinnamon essential oil against <i>S. pullorum</i>. Industrial Crops and Products, 2021-02-03.

[3]. Sheikh Shreaz, et al. Interesting anticandidal effects of anisic aldehydes on growth and proton-pumping-ATPase-targeted activity. Microb Pathog. 2011 Oct51(4):277-84.  

Chemical & Physical Properties

[ Density]:
1.1±0.1 g/cm3

[ Boiling Point ]:
243.5±0.0 °C at 760 mmHg

[ Molecular Formula ]:
C8H5D3O2

[ Molecular Weight ]:
139.166

[ Flash Point ]:
117.8±0.0 °C

[ Exact Mass ]:
139.071259

[ PSA ]:
26.30000

[ LogP ]:
1.72

[ Vapour Pressure ]:
0.0±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.547

[ Storage condition ]:
2-8°C

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

DownStream

Related Compounds