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(3-fluoro-phenyl)-(1-methyl-piperidin-4-yl)-amine, also known as 4'-fluoro-4-(1-methyl-4-piperidinyl)amino)-3-fluorophenylamine, is a complex chemical compound that features a fluorinated phenyl group connected to a piperidinylamine group. (3-fluoro-phenyl)-(1-methyl-piperidin-4-yl)-amine is recognized for its unique structure and chemical properties, which render it a valuable intermediate in the pharmaceutical industry for the synthesis of a variety of drugs and bioactive molecules.

36796-55-1

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36796-55-1 Usage

Uses

Used in Pharmaceutical Industry:
(3-fluoro-phenyl)-(1-methyl-piperidin-4-yl)-amine serves as a crucial building block in the synthesis of various pharmaceuticals and research chemicals. Its distinctive structure and reactivity make it instrumental in creating new drug candidates and advancing medicinal chemistry.
Due to the complex nature and potential reactivity of (3-fluoro-phenyl)-(1-methyl-piperidin-4-yl)-amine, it is essential to exercise proper handling and safety measures when working with (3-fluoro-phenyl)-(1-methyl-piperidin-4-yl)-amine in any application.

Check Digit Verification of cas no

The CAS Registry Mumber 36796-55-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,6,7,9 and 6 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 36796-55:
(7*3)+(6*6)+(5*7)+(4*9)+(3*6)+(2*5)+(1*5)=161
161 % 10 = 1
So 36796-55-1 is a valid CAS Registry Number.

36796-55-1Relevant academic research and scientific papers

4- ARYL(PIPERIDIN-4-YL)] AMINOBENZAMIDES WHICH BIND TO THE DELTA-OPIOID RECEPTOR

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Page/Page column 16-17, (2008/06/13)

4-[aryl(piperidin-4-yl)] aminobenzamides are delta-opioid receptor agonists/antagonists of formula (I). As delta-opioid receptor agonists, such compounds are useful as analgesics. Depending on their agonist/antagonist effect, such compounds may also be useful immunosuppressants, antiinflammatory agents, agents for the treatment of mental illness, medicaments for drug and alcohol abuse, agents for treating gastritis and diarrhea, cardiovascular agents, and agents for the treatment of respiratory diseases. In formula (I), [Ar is phenyl, 1-naphthyl or 2-naphthyl, each optionally substituted with 1 to 3 R; R - R are described in the application].

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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