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6-Chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amine is a chemical compound characterized by the molecular formula C7H5ClN4. It is a pyridine derivative featuring a triazolo ring and an amine group, which endows it with unique chemical properties and potential biological activity. This versatile compound is often utilized in pharmaceutical research and development due to its capacity to interact with various biological targets, making it a valuable asset in drug discovery endeavors.

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  • 1239647-60-9 Structure
  • Basic information

    1. Product Name: 6-chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amine
    2. Synonyms: 6-chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amine
    3. CAS NO:1239647-60-9
    4. Molecular Formula: C6H5ClN4
    5. Molecular Weight: 169
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1239647-60-9.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.: under inert gas (nitrogen or Argon) at 2–8 °C
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amine(1239647-60-9)
    11. EPA Substance Registry System: 6-chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amine(1239647-60-9)
  • 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: 1239647-60-9(Hazardous Substances Data)

1239647-60-9 Usage

Uses

Used in Pharmaceutical Research and Development:
6-Chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amine is employed as a key intermediate in the synthesis of new drug candidates. Its structure allows for the exploration of its interactions with different biological targets, which is crucial for identifying potential therapeutic agents.
Used in Drug Discovery:
In the pharmaceutical industry, 6-chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amine is used as a tool for drug discovery. The presence of the chlorine atom and the amine group in its molecule provides unique opportunities for chemical modifications, which can enhance its binding affinity to specific targets, thereby increasing its potential as a lead compound in drug development.
Used in Medicinal Chemistry:
6-Chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amine serves as a versatile building block in medicinal chemistry. Its chemical properties can be exploited to design and develop novel compounds with improved pharmacological profiles, including better potency, selectivity, and pharmacokinetic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 1239647-60-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,9,6,4 and 7 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1239647-60:
(9*1)+(8*2)+(7*3)+(6*9)+(5*6)+(4*4)+(3*7)+(2*6)+(1*0)=179
179 % 10 = 9
So 1239647-60-9 is a valid CAS Registry Number.

1239647-60-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-chloro-[1,2,4]triazolo[1,5-a]pyridin-2-amine

1.2 Other means of identification

Product number -
Other names 6-chloro[1,2,4]triazolo[1,5-a]pyridin-2-amine

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:1239647-60-9 SDS

1239647-60-9Relevant articles and documents

METHOD FOR PREPARING SUBSTITUTED TRIAZOLOPYRIDINES

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Paragraph 0531; 0532; 0533; 0534, (2015/06/03)

The present invention relates to methods of preparing substituted triazolopyridine compounds of general formula (I) as described and defined herein, as well as to intermediate compounds useful in the preparation of said compounds.

METHOD FOR PREPARING SUBSTITUTED TRIAZOLOPYRIDINES

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Page/Page column 111, (2014/02/15)

The present invention relates to methods o f preparing substituted triazolopyridine compounds of general formula (I) as described and defined herein, as well as to intermediate compounds useful in the preparation of said compounds.

SUBSTITUTED TRIAZOLOPYRIDINES HAVING ACTIVITY AS MPS-1 INHIBITORS

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Page/Page column 113-114, (2015/01/06)

The present invention relates to substituted triazolopyridine compounds of general formula (I), in which R1, R2, R3, R4, and R5 are as given in the description and in the claims, to methods of preparing said compounds, to pharmaceutical compositions and combinations comprising said compounds, to the use of said compounds for manufacturing a pharmaceutical composition for the treatment or prophylaxis of a disease, as well as to intermediate compounds useful in the preparation of said compounds.

PRODRUG DERIVATIVES OF SUBSTITUTED TRIAZOLOPYRIDINES

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Page/Page column 79, (2015/01/09)

The present invention relates to prodrug derivatives of Mps-1 kinase inhibitors, processes for their preparation, and their use for the treatment and/or prophylaxis of diseases.

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