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(S)-3-Fluoropiperidine hydrochloride is a chiral chemical compound belonging to the class of piperidines, characterized by a fluorine atom attached to the piperidine ring. It is typically found in the form of a white or off-white powder and is widely used in the pharmaceutical industry and organic synthesis.

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  • 871664-50-5 Structure
  • Basic information

    1. Product Name: (S)-3-Fluoropiperidine hy...
    2. Synonyms: (S)-3-Fluoropiperidine hy...;(S)-3-Fluoropiperidine hydrochloride;(3S)-3-fluoropiperidine hydrochloride;(S)-3-Fluoro-piperidine;(S)-3-FLUOROPIPERIDINE HCL
    3. CAS NO:871664-50-5
    4. Molecular Formula: C5H10FN*ClH
    5. Molecular Weight: 139.6
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 871664-50-5.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: (S)-3-Fluoropiperidine hy...(CAS DataBase Reference)
    10. NIST Chemistry Reference: (S)-3-Fluoropiperidine hy...(871664-50-5)
    11. EPA Substance Registry System: (S)-3-Fluoropiperidine hy...(871664-50-5)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 871664-50-5(Hazardous Substances Data)

871664-50-5 Usage

Uses

Used in Pharmaceutical Industry:
(S)-3-Fluoropiperidine hydrochloride is used as a building block in the synthesis of various pharmaceuticals and other organic compounds. Its unique structure and properties make it a valuable component in the development of new drugs.
Used in Organic Synthesis:
(S)-3-Fluoropiperidine hydrochloride is used as a chemical intermediate in organic synthesis, contributing to the production of other valuable chemicals.
Used in Research and Development:
(S)-3-Fluoropiperidine hydrochloride serves as a starting material for research and development in the field of chemistry, particularly in the exploration of new drug candidates and the synthesis of novel organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 871664-50-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,6,6 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 871664-50:
(8*8)+(7*7)+(6*1)+(5*6)+(4*6)+(3*4)+(2*5)+(1*0)=195
195 % 10 = 5
So 871664-50-5 is a valid CAS Registry Number.

871664-50-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (3S)-3-fluoropiperidine,hydrochloride

1.2 Other means of identification

Product number -
Other names (S)-3-FLUOROPIPERIDINE HYDROCHLORIDE

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:871664-50-5 SDS

871664-50-5Upstream product

871664-50-5Downstream Products

871664-50-5Relevant articles and documents

AMIDO-SUBSTITUTED AZOLE COMPOUNDS

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Page/Page column 207, (2015/11/02)

The present invention relates to amido-substituted azole compounds of general formula (I), in which X1, X2, R1, R2, R4, R5, R7 and R8 are as defined in the claims which are inhibitors of TNKS1 and/or TNKS2, to methods of preparing said compounds, to intermediate compounds useful for preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds and to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, in particular of neoplasms, as a sole agent or in combination with other active ingredients.

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