56248-49-8 Usage
Uses
Used in Pharmaceutical Industry:
2-METHOXY-D3-BENZALDEHYDE is used as a key intermediate for the synthesis of stilbene and dihydrostilbene derivatives, which are potential anticancer agents. These derivatives have shown promise in targeting and treating various types of cancer, making 2-METHOXY-D3-BENZALDEHYDE an essential component in the development of novel cancer treatments.
Used in Medicinal Chemistry:
2-METHOXY-D3-BENZALDEHYDE is also used in the synthesis of highly functionalized pyrrolidines, which are potent angiotensin-converting enzyme (ACE) inhibitors. These inhibitors play a crucial role in the regulation of blood pressure and have been widely used in the treatment of hypertension and other cardiovascular diseases. By contributing to the development of these inhibitors, 2-METHOXY-D3-BENZALDEHYDE holds significant value in the field of medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 56248-49-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,2,4 and 8 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56248-49:
(7*5)+(6*6)+(5*2)+(4*4)+(3*8)+(2*4)+(1*9)=138
138 % 10 = 8
So 56248-49-8 is a valid CAS Registry Number.
56248-49-8Relevant academic research and scientific papers
Cycloreversal reaction and ortho interactions in 2-Aryl-4H-3,1-benzoxazin-4-ones on electron
Ramana,Kantharaj
, p. 1195 - 1200 (2007/10/03)
A cycloreversal reaction, leading to aroyl cations, is the major process in 2-aryl-4H-3,1-benzoxazin-4-ones under electron impact conditions. The ortho interaction of the methoxy and the nitro groups in the 2-phenyl moieties in these compounds present the most abundant ions at m/z 119 and 134, respectively, in their mass spectra as a result of the transfer of a hydrogen atom from the former and an oxygen atom from the latter to the imine nitrogen of the heterocycle. The ion structures and the mechanisms for the proposed fragmentations are based on high-resolution data, B/E and B2/E linked-scan spectra, collision-activated decomposition-B-/E linked-scan spectra and deuterium labelling.
