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1-(azetidin-3-yl)-4,4-difluoropiperidine is a complex chemical compound that features an azetidine ring, a heterocyclic amine, and a piperidine ring, which is a common pharmacophore in pharmaceuticals. The presence of two fluorine atoms in its structure can significantly influence its biological activity. 1-(azetidin-3-yl)-4,4-difluoropiperidine is of interest in research and development, particularly in the pharmaceutical industry, due to the diverse physiological effects that azetidine and piperidine derivatives can exhibit.

1257293-83-6

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1257293-83-6 Usage

Uses

Used in Pharmaceutical Research and Development:
1-(azetidin-3-yl)-4,4-difluoropiperidine is used as a chemical intermediate for the synthesis of various pharmaceuticals, leveraging its azetidine and piperidine rings to explore a wide range of potential physiological effects. 1-(azetidin-3-yl)-4,4-difluoropiperidine's structure, including the fluorine atoms, may be further modified to enhance its properties and suitability for specific therapeutic applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(azetidin-3-yl)-4,4-difluoropiperidine is used as a building block for designing new drugs. Its unique structure allows for the creation of molecules with tailored properties, such as improved binding affinity to biological targets, increased stability, or enhanced bioavailability.
Used in Drug Discovery:
1-(azetidin-3-yl)-4,4-difluoropiperidine is employed in drug discovery as a potential lead compound. Its structural features make it a candidate for further optimization to develop new therapeutic agents, particularly in areas where azetidine and piperidine derivatives have shown promise, such as in the treatment of neurological disorders, pain management, or as antimicrobial agents.
Used in Chemical Synthesis:
In the broader field of chemical synthesis, 1-(azetidin-3-yl)-4,4-difluoropiperidine may be used as a reagent or a precursor in the preparation of more complex molecules. Its versatility in forming various chemical bonds and its potential for functional group transformations make it a valuable component in synthetic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 1257293-83-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,7,2,9 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1257293-83:
(9*1)+(8*2)+(7*5)+(6*7)+(5*2)+(4*9)+(3*3)+(2*8)+(1*3)=176
176 % 10 = 6
So 1257293-83-6 is a valid CAS Registry Number.

1257293-83-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(azetidin-3-yl)-4,4-difluoropiperidine

1.2 Other means of identification

Product number -
Other names 3-(4,4-DIFLUOROPIPERIDIN-1-YL)AZETANE

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1257293-83-6 SDS

1257293-83-6Upstream product

1257293-83-6Downstream Products

1257293-83-6Relevant academic research and scientific papers

7-(MORPHOLIN-4-YL)PYRAZOLE[1,5-A]PYRIMIDINE DERIVATIVES WHICH ARE USEFUL FOR THE TREATMENT OF IMMUNE OR INFLAMMATORY DISEASES OR CANCER

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Page/Page column 35-36, (2017/07/31)

A compound of the general formula (I) wherein Y represents -CH2- or >C=0; R1 is selected from the group consisting of A1, A2 and A3; R2 represents dioxothiomorpholino moiety B1, piperazinyl moiety B2, azetidinyl moiety B3, or piperidinyl moiety B4; R3 is selected from the group consisting of H, halogen, and C1 -C4 alkyl; R4 is selected from the group consisting of C1 -C4 alkyl, C3-C4- cycloalkyl, C1 -C4 alkyl substituted with C1 -C4 alkoxy, and CHF2, and their pharmaceutically acceptable salts. Pharmaceutical compositions comprising said compounds and their use in the treatment of diseases of immune system, inflammatory diseases and cancer.

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