CAS 579-72-6
:2-(Dimethylamino)benzaldehyde
- 2-(N,N-Dimethylamino)benzaldehyde
- Anthranilaldehyde, N,N-dimethyl-
- Benzaldehyde, 2-(dimethylamino)-
- N,N-Dimethylanthranilaldehyde
- o-(Dimethylamino)benzaldehyde
- 2-(Dimethylamino)benzaldehyde
- 2-(Dimethylamino)benzaldehyde97%
- N,N-Dimethyl-2-formylaniline, N,N-Dimethylanthranilaldehyde
- 2-(Dimethylamino)benzaldehyde 97%
2-(Dimethylamino)benzaldehyde
CAS:Formula:C9H11NOPurity:98%Color and Shape:LiquidMolecular weight:149.18972-(Dimethylamino)benzaldehyde
CAS:2-(Dimethylamino)benzaldehydeFormula:C9H11NOPurity:97%Color and Shape: clear. light green to yellow liquidMolecular weight:149.19g/mol2-(N,N-Dimethylamino)benzaldehyde
CAS:Formula:C9H11NOPurity:98%Color and Shape:LiquidMolecular weight:149.1932-(N,N-Dimethylamino)benzaldehyde
CAS:Controlled ProductApplications 2-(N,N-Dimethylamino)benzaldehyde
Formula:C9H11NOColor and Shape:NeatMolecular weight:149.192-(Dimethylamino)benzaldehyde
CAS:2-(Dimethylamino)benzaldehyde is a stilbene derivative. It inhibits the activity of an enzyme called tyrosine phosphatase by binding to the active site of the enzyme and blocking its catalytic function. This compound has been used in vitro studies to study autoimmune diseases and may have potential as a drug for rheumatoid arthritis. 2-(Dimethylamino)benzaldehyde also binds to influenza virus, stabilizing it and inhibiting its replication, but does not inhibit other viruses such as HIV-1 or poliovirus.2-(Dimethylamino)benzaldehyde can be prepared by reacting n-dimethylformamide with hydrochloric acid. The reaction produces hydrogen chloride gas, which is then bubbled through redox potentials (e.g., ferric chloride solution), yielding 2-(dimethylamino)benzaldehyde and hydrogen gas.
2-(Dimethylamino)benzaldehyde can be synthesized usingFormula:C9H11NOPurity:Min. 95%Molecular weight:149.19 g/mol





