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(4-CHLORO-PHENYL)-PIPERIDIN-4-YL-AMINE, a chemical compound with the molecular formula C11H15ClN2, is a piperidine derivative featuring a 4-chloro-phenyl group attached to the piperidine ring. (4-CHLORO-PHENYL)-PIPERIDIN-4-YL-AMINE is recognized for its role as an intermediate in the synthesis of pharmaceuticals and agrochemicals, and it is instrumental in the production of various medications, including antipsychotic and antihistamine drugs. Its chemical structure and properties render it a valuable building block for the synthesis of biologically active compounds, making it a significant component in research and development for the discovery of new therapeutic agents.

37656-67-0

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37656-67-0 Usage

Uses

Used in Pharmaceutical Industry:
(4-CHLORO-PHENYL)-PIPERIDIN-4-YL-AMINE is used as a key intermediate in the synthesis of various medications, primarily for its role in creating antipsychotic and antihistamine drugs. Its unique structure allows for the development of compounds that can effectively target and modulate specific receptors in the body, contributing to the treatment of mental health disorders and allergic reactions.
Used in Agrochemical Industry:
In the agrochemical sector, (4-CHLORO-PHENYL)-PIPERIDIN-4-YL-AMINE serves as an intermediate in the production of pesticides and other crop protection agents. Its chemical properties enable the creation of compounds that can protect crops from pests and diseases, thereby ensuring food security and agricultural productivity.
Used in Research and Development:
(4-CHLORO-PHENYL)-PIPERIDIN-4-YL-AMINE is utilized as a building block in the research and development of new therapeutic agents. Its chemical structure provides a foundation for the design and synthesis of innovative compounds with potential applications in various medical fields, including the treatment of neurological disorders, cardiovascular diseases, and other health conditions.
Overall, (4-CHLORO-PHENYL)-PIPERIDIN-4-YL-AMINE is a versatile chemical compound with significant applications across different industries, particularly in the development and production of pharmaceuticals and agrochemicals, as well as in scientific research for the advancement of new therapeutic agents.

Check Digit Verification of cas no

The CAS Registry Mumber 37656-67-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,6,5 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 37656-67:
(7*3)+(6*7)+(5*6)+(4*5)+(3*6)+(2*6)+(1*7)=150
150 % 10 = 0
So 37656-67-0 is a valid CAS Registry Number.

37656-67-0Relevant academic research and scientific papers

MULTIVALENT RAS BINDING COMPOUNDS

-

, (2017/07/23)

Described herein are compounds that modulate Ras signaling, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds, and methods of using such compounds in the treatment of conditions, diseases, or disorders associated with altered Ras signaling. Further described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments comprising such compounds and methods of using such compounds in the treatment of cell proliferative disorders, including cancer.

NOVEL ANTIFUNGAL TRIAZOLE DERIVATIVES

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, (2012/12/14)

Disclosed are novel triazole derivatives. Exhibiting excellent antifungal activity and in vivo safety, they are useful for the treatment or prevention of fungal infections caused by a wide spectrum of fungi.

NOVEL ANTIFUNGAL TRIAZOLE DERIVATIVES

-

, (2011/09/15)

Disclosed are novel triazole derivatives. Exhibiting excellent antifungal activity and in vivo safety, they are useful for the treatment or prevention of fungal infections caused by a wide spectrum of fungi.

PIPERIDINE DERIVATIVES USEFUL AS HISTAMINE H3 ANTAGONISTS

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Page/Page column 40-41, (2010/11/25)

Disclosed are novel compounds of the formula (I) or a pharmaceutically acceptable salt thereof, wherein: M1 and M3 are CH or N; M2 is CH, CF or N; Y is -C(=O)-, -C(=S)-, -(CH2)q-, -C(=NOR7)

COMPOUNDS USEFUL AS CHEMOKINE RECEPTOR ANTAGONISTS

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Page/Page column 112, (2008/06/13)

The present invention relates to compounds useful as Chemokine Receptor antagonists. Compounds of general formula (I) are provided or pharmaceutically acceptable salts thereof. The invention also provides pharmaceutically acceptable compositions comprising said compounds and methods of using the compounds and compositions for the inhibition of Chemokine Receptors and also for the treatment of various diseases, conditions, or disorders, including acute or chronic inflammatory disease, cancer, and osteolytic bone disorders.

Novel compounds

-

, (2008/06/13)

The invention provides compounds of general formula (I) wherein Q, R, R2, R4, R5, R6, R7 and R8 are as defined in the specification, processes for their preparation, pharmaceutical compositions containing them and their use in therapy.

New 4-arylaminopiperidines with antihypoxic and anticonvulsive activity

Domany,Barta-Szalai,Palosi,Szabo,Schon

, p. 989 - 991 (2007/10/02)

Several new bioanalogues of (±)-N-methyl-N-{1-[3-(4-fluorophenoxy)-2-hydroxy-propyl]piperidin-4- yl}benzothiazol-2-amine (1, sabeluzole, CAS 104383-17-7) were prepared by reacting 1,2-epoxy-3-aryloxypropanes with 4-arylaminopiperidines. Some of these derivatives showed enhanced activity in the potassium cyanide hypoxia test and in the pentetrazol convulsion test in mice compared to 1.

Aminohaloborane in Organic Synthesis. IX. Exclusive ortho Acylation Reaction of N-Monoaminoalkylanilines

Adachi, Makoto,Sasakura, Kazuyuki,Sugasawa, Tsutomu

, p. 1826 - 1835 (2007/10/02)

The exclusive ortho acylation reaction of aniline derivatives using boron trichloride made possible the one-step synthesis of 2-acyl-N-monoaminoalkylanilines (1) and the corresponding imines (2) from N-monoaminoalkylanilines, even in the case of compounds with a bulky substituent at the nitrogen atom.Conventional methods only give 1 via elaborate procedures.Keywords: regioselective reaction; 2-acylaniline derivative; 2-acylaniline-imine derivative; boron trichloride

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