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(2R,3R)-3-(Benzyl-methyl-amino)-2-phenyl-chroman-4-one is a complex organic compound with a molecular formula of C23H23NO2. It is a chiral molecule, meaning it has a non-superimposable mirror image, and the specific configuration is indicated by the (2R,3R) notation. (2R,3R)-3-(Benzyl-methyl-amino)-2-phenyl-chroman-4-one features a chroman-4-one core, which is a type of chromone with a carbonyl group at the 4-position. The molecule also includes a benzyl-methyl-amino group attached to the 3-position, and a phenyl group at the 2-position. This structure is significant in the field of medicinal chemistry, as it may exhibit biological activity or serve as a precursor in the synthesis of pharmaceuticals. The specific properties and applications of (2R,3R)-3-(Benzyl-methyl-amino)-2-phenyl-chroman-4-one would depend on its ability to interact with biological targets, such as enzymes or receptors, which could make it a potential candidate for drug development or as a research tool in studying biochemical pathways.

81281-84-7

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81281-84-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81281-84-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,8 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81281-84:
(7*8)+(6*1)+(5*2)+(4*8)+(3*1)+(2*8)+(1*4)=127
127 % 10 = 7
So 81281-84-7 is a valid CAS Registry Number.

81281-84-7Downstream Products

81281-84-7Relevant academic research and scientific papers

FLAVONOIDS, XXXVI REACTION OF 3-ALKYL- OR -ARYLSULFONYLOXYFLAVANONES WITH AMINES. SYNTHESIS OF 3-DIALKYLAMINOFLAVANONES

Patonay, T.,Litkei, Gy.,Bognar, R.

, p. 135 - 146 (2007/10/02)

Reactions of 3-alkyl- or -arylsulfonyloxyflavanones (1a-h) with primary and tertiary amines gave mixtures of the corresponding flavones (2a-d) and aurones (3a-d), while with secondary amines, in addition to 2 and 3, 3-dialkylaminoflavanones (6-9) were also obtained.The factors which determine the ratio of products are discussed.Treatment of the 3-dialkylaminoflavones 6a and 7 with DDQ gave 3-dialkylaminoflavanones (10, 11); treatment with alkali in methanol afforded 2-dialkylamino-2-benzylcoumaran-3-ones (12, 13).

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