873384-32-8 Usage
Appearance
Yellow to brown crystalline solid The compound has a yellow to brown color and a crystalline structure.
Usage
Building block for organic synthesis It is used as a starting material in the creation of other chemicals and pharmaceuticals.
Structural features
Two bromine atoms The compound contains two bromine atoms attached to the benzene ring, which can be important for its reactivity and properties.
Functional group
Aldehyde The compound has an aldehyde functional group (-CHO), which is essential for its use in organic synthesis and reactions.
Intermediate compound
Used in the production of pharmaceuticals and organic compounds 2,6-dibromo-3,4-dimethoxybenzaldehyde is often used as an intermediate in the synthesis of various pharmaceuticals and organic compounds.
Potential applications
Antimicrobial and anti-tumor The compound has been studied for its potential use in antimicrobial and anti-tumor applications, which could make it valuable in the development of new treatments for infections and cancer.
Check Digit Verification of cas no
The CAS Registry Mumber 873384-32-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,3,3,8 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 873384-32:
(8*8)+(7*7)+(6*3)+(5*3)+(4*8)+(3*4)+(2*3)+(1*2)=198
198 % 10 = 8
So 873384-32-8 is a valid CAS Registry Number.
873384-32-8Relevant academic research and scientific papers
Palladium-catalyzed ortho-C(sp2)[sbnd]H bromination of benzaldehydes via a monodentate transient directing group strategy
Yong, Qiyun,Sun, Bing,Zhang, Fang-Lin
supporting information, (2019/11/03)
A facile and efficient monodentate transient directing group strategy was developed to enable the palladium-catalyzed ortho-C(sp2)[sbnd]H bromination of benzaldehydes. A broad scope of benzaldehydes were transformed into the desired products by employing 2-amino-5-chlorobenzotrifluoride as a monodentate transient directing group, demonstrating good functional group tolerance. Mild reaction conditions and no requirement for a silver salt are also features of this strategy.
