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(S)-N-(2-oxochroman-3-yl)benzamide is a chiral compound belonging to the class of benzamides, characterized by the presence of a benzene ring and an amide functional group. The molecule features a 2-oxochroman-3-yl moiety, which is derived from chromanone, a heterocyclic compound with a benzene ring fused to a pyran ring and a carbonyl group at the 2-position. The (S)-configuration indicates that the molecule has a specific arrangement of atoms around the chiral center, which is crucial for its biological activity and potential applications. (S)-N-(2-oxochroman-3-yl)benzamide may have potential applications in pharmaceuticals or as a chiral building block in organic synthesis, given its unique structure and stereochemistry.

35175-73-6

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35175-73-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 35175-73-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,5,1,7 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 35175-73:
(7*3)+(6*5)+(5*1)+(4*7)+(3*5)+(2*7)+(1*3)=116
116 % 10 = 6
So 35175-73-6 is a valid CAS Registry Number.

35175-73-6Downstream Products

35175-73-6Relevant academic research and scientific papers

Rhodium-Catalyzed Asymmetric Hydrogenation of 3-Benzoylaminocoumarins for the Synthesis of Chiral 3-Amino Dihydrocoumarins

Xu, Yunnan,Liu, Delong,Deng, Yu,Zhou, Yi,Zhang, Wanbin

, p. 23602 - 23607 (2021/10/05)

An asymmetric hydrogenation of 3-benzoylaminocoumarins was achieved for the first time using our BridgePhos-Rh catalytic system, providing chiral 3-amino dihydrocoumarins in high yields (up to 98 %) and with excellent enantioselectivities (up to 99.7 % ee). The relationship between the enantioselectivities of the hydrogenations and the dihedral angles and the resulting π-π stacking effects of the BridgePhos-Rh complexes, which were determined by X-ray diffraction analysis, are discussed. The corresponding hydrogenated products allow for many transformations, providing several chiral skeletons with important physiological and pharmacological activities.

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