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(S)-N-(chroman-3-yl)benzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1315549-67-7

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1315549-67-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1315549-67-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,5,5,4 and 9 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1315549-67:
(9*1)+(8*3)+(7*1)+(6*5)+(5*5)+(4*4)+(3*9)+(2*6)+(1*7)=157
157 % 10 = 7
So 1315549-67-7 is a valid CAS Registry Number.

1315549-67-7Downstream Products

1315549-67-7Relevant academic research and scientific papers

Efficient enantioselective synthesis of 3-aminochroman derivatives through ruthenium-synphos catalyzed asymmetric hydrogenation

Wu, Zi,Ayad, Tahar,Ratovelomanana-Vidal, Virginie

, p. 3782 - 3785 (2011)

A highly enantioselective asymmetric hydrogenation of various trisubstituted enamides derived from chroman-3-ones promoted by cationic Ru-Synphos catalysts is reported. This atom-economical and clean method provides an efficient route to optically active

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

supporting information, 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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