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(R)-3-(3-hydroxypropyl)-3-methyl-1-phenyl-3,4-dihydro-1H-quinoline-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1006614-08-9

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1006614-08-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1006614-08-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,6,1 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1006614-08:
(9*1)+(8*0)+(7*0)+(6*6)+(5*6)+(4*1)+(3*4)+(2*0)+(1*8)=99
99 % 10 = 9
So 1006614-08-9 is a valid CAS Registry Number.

1006614-08-9Upstream product

1006614-08-9Downstream Products

1006614-08-9Relevant academic research and scientific papers

Atropisomeric lactam chemistry: catalytic enantioselective synthesis, application to asymmetric enolate chemistry and synthesis of key intermediates for NET inhibitors

Takahashi, Masashi,Tanabe, Hajime,Nakamura, Tsuyoshi,Kuribara, Daisuke,Yamazaki, Toshiyuki,Kitagawa, Osamu

, p. 288 - 296 (2010)

In the presence of (R)-SEGPHOS-Pd(OAc)2 catalyst, the intramolecular N-arylation of ortho-tert-butyl-NH-anilides possessing an iodophenyl group proceeded in a highly enantioselective manner (89-98% ee) to give optically active atropisomeric lac

Catalytic enantioselective synthesis of key intermediates for NET inhibitors using atropisomeric lactam chemistry

Kitagawa, Osamu,Kurihara, Daisuke,Tanabe, Hajime,Shibuya, Taichi,Taguchi, Takeo

, p. 471 - 474 (2008/09/17)

An atropisomeric lactam which was prepared with high enantioselectivity by catalytic asymmetric intramolecular N-arylation, was efficiently converted to synthetic intermediates for NET inhibitors through highly diastereoselective α-alkylation followed by

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