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tert-butyl (6-(cyclohexylamino)hexyl)carbamate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

239064-32-5

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239064-32-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 239064-32-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,9,0,6 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 239064-32:
(8*2)+(7*3)+(6*9)+(5*0)+(4*6)+(3*4)+(2*3)+(1*2)=135
135 % 10 = 5
So 239064-32-5 is a valid CAS Registry Number.

239064-32-5Relevant academic research and scientific papers

Highly Selective Reductive Cross-Amination between Aniline or Nitroarene Derivatives and Alkylamines Catalyzed by Polysilane-Immobilized Rh/Pt Bimetallic Nanoparticles

Suzuki, Aya,Miyamura, Hiroyuki,Kobayashi, Shu

supporting information, p. 387 - 392 (2019/02/26)

Reductive cross-amination between imine intermediates generated through partial hydrogenation of aniline or nitroarene derivatives and alkylamines is an ideal method for obtaining N-alkylated cyclohexylamine derivatives; however, no such transformations have hitherto been established. Here, we report a highly selective reductive cross-amination using aniline derivatives and alkylamines catalyzed by heterogeneous Rh/Pt bimetallic nanoparticles under mild conditions. The catalyst was recovered and reused for five runs, keeping high activity. In this reaction, imine intermediates generated during the course of partial hydrogenation of aniline derivatives were trapped immediately by strongly interacting primary alkylamines with the catalyst, which caused a highly selective transformation to give the desired products, while suppressing dicyclohexylamine formation.

4-heterocyclohexanone-based inhibitors of the serine protease plasmin

Sanders, Tanya C.,Seto, Christopher T.

, p. 2969 - 2976 (2007/10/03)

Three inhibitors that are based upon a 4-heterocyclohexanone nucleus were synthesized and evaluated for activity against the serine protease plasmin. Inhibitors of plasmin have potential as cancer chemotherapeutic agents that act by blocking both angiogen

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