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(1S,2R)-(-)-cis-1-[(2S,4S,6R)-4-hydroxymethyl-6-methyl-2-phenylpiperidin-1-yl]-7-isopropylindan-2-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

910106-26-2

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910106-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 910106-26-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,1,0 and 6 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 910106-26:
(8*9)+(7*1)+(6*0)+(5*1)+(4*0)+(3*6)+(2*2)+(1*6)=112
112 % 10 = 2
So 910106-26-2 is a valid CAS Registry Number.

910106-26-2Downstream Products

910106-26-2Relevant articles and documents

Stereocontrolled synthesis of substituted chiral piperidines viaone-pot asymmetric 6π-azaelectrocyclization: Asymmetric syntheses of(-)-dendroprimine, (+)-7-epidendroprimine, (+)-5-epidendroprimine, and (+)-5,7-epidendroprimine

Kobayashi, Toyoharu,Hasegawa, Futoshi,Hirose, Yoshikatsu,Tanaka, Katsunori,Mori, Hajime,Katsumura, Shigeo

, p. 1812 - 1832 (2012/04/04)

The asymmetric one-pot 6π-azaelectrocyclization of alkenyl vinyl stannane, ethyl (Z)-2-iodo-4-oxobutenoate, and (-)-7-isopropyl-cis-aminoindanol in the presence of a Pd(0) catalyst stereoselectively produced the tetracyclic aminoacetal compounds, resultin

Synthesis of 2,4,6-trisubstituted chiral piperidines and (-)-dendroprimine by one-pot asymmetric azaelectrocyclization protocol

Kobayashi, Toyoharu,Hasegawa, Futoshi,Tanaka, Katsunori,Katsumura, Shigeo

, p. 3813 - 3816 (2007/10/03)

Stereocontrolled synthesis of 2,4,6-trisubstituted piperidine diastereomers has been realized from common intermediates, obtained by a one-pot azaelectrocyclization protocol. Based on the method, the asymmetric synthesis of an indolizidine alkaloid, (-)-d

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