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Piperidine, 3-(1H-1,2,4-triazol-1-yl)(9CI), also known as 1-(3-piperidin-1-ylpropyl)-1H-1,2,4-triazole, is a chemical compound that features both piperidine and 1H-1,2,4-triazol-1-yl groups. Piperidine, 3-(1H-1,2,4-triazol-1-yl)(9CI) is recognized for its potential as a drug intermediate, playing a crucial role in the synthesis of various pharmaceuticals. Its unique structure and properties have garnered interest in the pharmaceutical industry due to its potential therapeutic applications, although further research and testing are necessary to fully explore its capabilities and effects.

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  • 774511-83-0 Structure
  • Basic information

    1. Product Name: Piperidine, 3-(1H-1,2,4-triazol-1-yl)- (9CI)
    2. Synonyms: Piperidine, 3-(1H-1,2,4-triazol-1-yl)- (9CI);3-(1H-1,2,4-triazol-1-yl)piperidine
    3. CAS NO:774511-83-0
    4. Molecular Formula: C7H12N4
    5. Molecular Weight: 152.19698
    6. EINECS: N/A
    7. Product Categories: METHYL
    8. Mol File: 774511-83-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 306.7±52.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.34±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 8.52±0.10(Predicted)
    10. CAS DataBase Reference: Piperidine, 3-(1H-1,2,4-triazol-1-yl)- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Piperidine, 3-(1H-1,2,4-triazol-1-yl)- (9CI)(774511-83-0)
    12. EPA Substance Registry System: Piperidine, 3-(1H-1,2,4-triazol-1-yl)- (9CI)(774511-83-0)
  • 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: 774511-83-0(Hazardous Substances Data)

774511-83-0 Usage

Uses

Used in Pharmaceutical Industry:
Piperidine, 3-(1H-1,2,4-triazol-1-yl)(9CI) is used as a drug intermediate for the synthesis of various pharmaceuticals, contributing to the development of new medications and therapies.
Used in Research and Development:
In the realm of research and development, Piperidine, 3-(1H-1,2,4-triazol-1-yl)(9CI) serves as a valuable compound for exploring and creating novel drug candidates, potentially leading to breakthroughs in medicinal chemistry and therapeutics.
While the provided materials do not specify distinct applications in different industries or detailed reasons for each application, the general uses outlined above reflect the compound's role in the pharmaceutical sector and its potential for future development. Further exploration and studies are essential to delineate specific applications and industries where this compound could be effectively utilized.

Check Digit Verification of cas no

The CAS Registry Mumber 774511-83-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,7,4,5,1 and 1 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 774511-83:
(8*7)+(7*7)+(6*4)+(5*5)+(4*1)+(3*1)+(2*8)+(1*3)=180
180 % 10 = 0
So 774511-83-0 is a valid CAS Registry Number.

774511-83-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(1H-1,2,4-triazol-1-yl)piperidine

1.2 Other means of identification

Product number -
Other names 3-(1H-1,2,4-TRIAZOL-1-YL)PIPERIDINE

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:774511-83-0 SDS

774511-83-0Downstream Products

774511-83-0Relevant articles and documents

A convenient synthesis of (1 H-azol-1-yl)piperidines

Shevchuk, Nadiia V.,Liubchak, Kostiantyn,Nazarenko, Kostiantyn G.,Yurchenko, Aleksandr A.,Volochnyuk, Dmitriy M.,Grygorenko, Oleksandr O.,Tolmachev, Andrey A.

experimental part, p. 2041 - 2048 (2012/08/07)

A convenient preparation of 3- and 4-(1H-azol-1-yl)piperidines by arylation of azoles (i.e., pyrazoles, imidazoles, and triazoles) with 3- and 4-bromopyridines and subsequent reduction of the pyridine ring was developed. The method was extended to benzo analogues of the title compounds. Georg Thieme Verlag Stuttgart · New York.

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