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2-(4-chlorophenyl)-1,3-propanediamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

114703-75-2

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114703-75-2 Usage

Chemical family

Diamine

Biological role

Microtubule destabilizing agent

Mechanism of action

Binds to beta-tubulin subunits in microtubules and prevents their polymerization

Effects on cells

Disruption of microtubule network, cell cycle arrest

Research applications

Studying the role of microtubules in cellular processes such as mitosis and cell migration

Therapeutic potential

Anti-cancer properties, being investigated for use in cancer therapy

Check Digit Verification of cas no

The CAS Registry Mumber 114703-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,7,0 and 3 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 114703-75:
(8*1)+(7*1)+(6*4)+(5*7)+(4*0)+(3*3)+(2*7)+(1*5)=102
102 % 10 = 2
So 114703-75-2 is a valid CAS Registry Number.

114703-75-2Relevant academic research and scientific papers

KINASE INHIBITORS

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Paragraph 0084-0085, (2013/12/03)

The present invention relates to compounds of Formula I or a pharmaceutically acceptable salt thereof, wherein variables R, Ar, X, and Ar1 and n are as defined herein. The compounds are capable of modulating tyrosine kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation.

Synthesis of optically active heterocyclic compounds by preparation of 1,3-dinitro derivatives and enzymatic enantioselective desymmetrization of prochiral diamines

Rios-Lombardia, Nicolas,Busto, Eduardo,Gotor-Fernandez, Vicente,Gotor, Vicente

experimental part, p. 484 - 493 (2010/04/28)

A general approach for the highly efficient chemical preparation of novel optically active 2-substituted propane-1,3-diamines is described. Diamines have been obtained from the corresponding commercially available aldehydes in a straightforward, two-step synthesis via the corresponding 1,3-dinitro compounds, which were hydrogenated under mild reaction conditions by using platinum dioxide as the catalyst. Subsequent enzymatic enantioselective desymmetrization mediated by Pseudomonas cepacia lipase allowed the recovery of a family of monocarbamates in good to high, enantiomeric excesses (70-90% ee).

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