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(1R,2R)-1-methyl-2-phenyl-propylamine is a chiral secondary amine with the molecular formula C??H??N. It is characterized by a methyl group at the first carbon, a phenyl group at the second carbon, and an amine group at the third carbon. The compound exhibits two chiral centers, which are the first and second carbon atoms, resulting in four possible stereoisomers. The specific (1R,2R) configuration indicates that both chiral centers have the R (rectus) configuration, meaning that the substituents at these centers follow the clockwise priority order when viewed from the perspective of the amine group. (1R,2R)-1-methyl-2-phenyl-propylamine is of interest in the field of organic chemistry, particularly in the synthesis of pharmaceuticals and other chiral molecules, due to its unique stereochemistry and potential applications in asymmetric synthesis.

33603-05-3

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33603-05-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33603-05-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,6,0 and 3 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33603-05:
(7*3)+(6*3)+(5*6)+(4*0)+(3*3)+(2*0)+(1*5)=83
83 % 10 = 3
So 33603-05-3 is a valid CAS Registry Number.

33603-05-3Relevant academic research and scientific papers

Asymmetric reduction of nitroalkenes with baker's yeast

Kawai, Yasushi,Inaba, Yoshikazu,Tokitoh, Norihiro

, p. 309 - 318 (2007/10/03)

Various α,β-disubstituted and trisubstituted nitroalkenes were chemoselectively reduced with baker's yeast to the corresponding nitroalkanes. Stereoselectivities of the reduction of α,β-disubstituted nitroalkenes were modest to low, and e.e.s up to 52% were obtained. Trisubstituted nitroalkenes could be reduced to the corresponding nitroalkanes with excellent enantioselectivities, moderate diastereoselectivities and in good yield.

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