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E/Z-2-(RS)-N-[(R)-1-phenylethyl]-2-methylcyclopentylideneamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

309756-60-3

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309756-60-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 309756-60-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,9,7,5 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 309756-60:
(8*3)+(7*0)+(6*9)+(5*7)+(4*5)+(3*6)+(2*6)+(1*0)=163
163 % 10 = 3
So 309756-60-3 is a valid CAS Registry Number.

309756-60-3Relevant articles and documents

Stereoselective Michael additions on α-aminoacrylates as the key step to an l-Oic analogue bearing a quaternary stereocenter

Cecchinelli, Federico Maria,Celentano, Giuseppe,Gaggero, Nicoletta,Puglisi, Alessandra

, p. 671 - 674 (2020)

A novel, highly stereoselective route for pharmaceutically relevant octahydroindole-2-carboxylates bearing a quaternary stereocenter has been developed. The key chiral intermediates 3 have been prepared in good yields and enantiomeric excesses up to 98%. A broad substrate range has been tolerated under the reaction conditions.

Intramolecular reductive ketone-alkynoate coupling reaction promoted by (η2-propene)titanium

Schaefer, Christian,Miesch, Michel,Miesch, Laurence

supporting information; scheme or table, p. 3253 - 3257 (2012/06/01)

Intramolecular reductive coupling of cycloalkanones tethered to alkynoates in the presence of (η2-propene)titanium was successfully performed to provide hydroxy-esters in a diastereoselective manner. Subsequent lactonization afforded angularly

Enantioselective synthesis of a simple benzenoid analogue of glycinoeclepin a

Giroux, Simon,Corey

supporting information; experimental part, p. 5617 - 5619 (2009/06/18)

(Chemical Equation Presented) A synthesis of the readily accessible glycinoeclepin A analogue 2 is reported.

Carbocyclic α-amino acids: Asymmetric Strecker synthesis of a series of 2-alkylated 1-aminocyclopentanecarboxylic acids

Wede, Judith,Volk, Franz-J.,Frahm, August W.

, p. 3231 - 3252 (2007/10/03)

A series of 12 carbocyclic α-amino acids has been prepared from four different racemic 2-alkylated cyclopentanones and (R)-1-phenylethylamine as the chiral auxiliary by means of an asymmetric Strecker synthesis. The stereoselectivity was influenced by sol

Asymmetric Reductive Amination of Cycloalkanones, 5. Synthesis and Absolute Configuration of 2-Substituted Cyclopentanamines

Wiehl, Wolfgang,Frahm, August W.

, p. 2668 - 2677 (2007/10/02)

In an asymmetric synthesis 2-substituted cyclopentanamines are obtained from racemic cyclopentanones by means of reductive amination in a three-step procedure.Condensation of the ketones 3(n) with optically active 1-phenylethylamines yields imine mixtures

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