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Trans-(5S,6S)-4,5-dimethyl-2,6-diphenyl-5,6-dihydro-4H-1,3,4-oxadiazine is a complex organic compound characterized by its unique molecular structure. It is a chiral molecule, meaning it has a non-superimposable mirror image, with the specific configuration being the trans-(5S,6S) form. The compound features a 1,3,4-oxadiazine ring, which is a six-membered ring containing two nitrogen atoms and one oxygen atom. The molecule also includes two methyl groups at the 4 and 5 positions, and two phenyl groups at the 2 and 6 positions, which are part of the dihydro structure, indicating the presence of two hydrogen atoms attached to the carbon atoms of the ring. trans-(5S,6S)-4,5-dimethyl-2,6-diphenyl-5,6-dihydro-4H-1,3,4-oxadiazine is significant in the field of organic chemistry, potentially serving as a building block for more complex molecules or having applications in pharmaceuticals or materials science.

4826-46-4

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4826-46-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4826-46-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,2 and 6 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 4826-46:
(6*4)+(5*8)+(4*2)+(3*6)+(2*4)+(1*6)=104
104 % 10 = 4
So 4826-46-4 is a valid CAS Registry Number.

4826-46-4Downstream Products

4826-46-4Relevant academic research and scientific papers

Synthesis and X-ray crystal structures of chiral, nonracemic 5,6-dihydro-4H-1,3,4-oxadiazines

Hitchcock, Shawn R.,Dean, Melissa A.,Kelley, Christopher J.,Edler, Kate L.,Ferrence, Gregory M.

scheme or table, p. 982 - 989 (2010/09/03)

A series of chiral, nonracemic oxadiazines have been prepared from (1R,2S)-ephedrine, (1R,2S)-norephedrine, and L-phenylalaninol. The synthesis of the Ephedra-based oxadiazines was accomplished by a process of N-nitrosation, reduction, acylation, and acid

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