CAS 591-31-1
:3-Methoxybenzaldehyde
- 3-Anisaldehyd
- 3-Anisaldehyde
- 3-Methoxy-Benzaldehyd
- 3-Methoxybenxaldehyde
- 3-Methoxybenzaldehde
- 3-Methoxybenzaldehyd
- 3-Methoxyphenylcarboxaldehyde
- 3-Metoxibenzaldehido
- Akos Bbs-00003247
- Anisaldehyde,3-
- Benzaldehyde, 3-methoxy-
- Benzaldehyde, m-methoxy-
- M-Anisadehyde
- M-Anisaldehyde
- M-Methoxybenzaldehyde
- Meta-Anisaldehyd
- Meta-Anisaldehyde
- Metamethoxybenzaldehyde
- Nsc 43794
- Phenanthro[1,2-B]Thiophene
- See more synonyms
m-Anisaldehyde
CAS:Formula:C8H8O2Purity:>98.0%(GC)Color and Shape:Colorless to Light orange to Yellow clear liquidMolecular weight:136.153-Methoxybenzaldehyde, 98%
CAS:3-Methoxybenzaldehyde is used to prepare 3-(3-methoxy-phenyl)-1-phenyl-propenone by reaction with benzldehyde. It is used as an eluent for mono-13C isotopomers of vanillin in normal phase silica gel chromatography. It acts as an inhibitor of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanone (NNK) metab
Formula:C8H8O2Purity:98%Color and Shape:Clear colorless to yellow, LiquidMolecular weight:136.153-Methoxybenzaldehyde
CAS:3-MethoxybenzaldehydeFormula:C8H8O2Purity:98%Color and Shape: clear. colourless liquidMolecular weight:136.15g/molm-Anisaldehyde
CAS:m-Anisaldehyde exhibits binding activity toward aldo-keto reductase family 1 member A1 and is widely used in biochemical experimentsFormula:C8H8O2Purity:99.73%Color and Shape:SolidMolecular weight:136.153-Methoxybenzaldehyde
CAS:Applications 3-Methoxybenzaldehyde is a reagent used in the synthesis of substrate inhibitors of acylated quinoline N-oxides. Also used in organic synthesis involving potent heterodimeric modulators of breast cancer resistance protein.
References Chen, X. et al.: Org. Lett., 18, 2411 (2016); Kraege, S. et al.: Eur. J. Med. CHem., 117, 212 (2016);Formula:C8H8O2Color and Shape:NeatMolecular weight:136.153-Methoxybenzaldehyde
CAS:3-Methoxybenzaldehyde is a chemical compound that is used as an intermediate in the synthesis of organic compounds. This compound has shown to be a potent inhibitor of several enzymes, including diamine tetraacetic acid (DAT)-dependent aminotransferase, trimethyl amine N-oxide reductase, and hydrochloric acid hydrolases. 3-Methoxybenzaldehyde also inhibits the growth of hepg2 cells and induces apoptosis. The chemical structure of this compound contains a boron nitride group that can form hydrogen bonds with other molecules and fatty acids that can act as a substrate for oxidation reactions.
Formula:C8H8O2Purity:Min. 98 Area-%Color and Shape:Clear LiquidMolecular weight:136.15 g/mol







