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6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine is a synthetic compound that belongs to the class of organic compounds known as methoxytriazolopyridines. It is characterized by a 6-membered pyridine ring fused to a 1,2,4-triazole ring on one side, with a methoxy group substitution at the 6th position. The specific chemical features of this compound can influence its reactivity and overall behavior in diverse chemical or biological systems.

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  • 1092394-15-4 Structure
  • Basic information

    1. Product Name: 6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine
    2. Synonyms: 6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine;6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-ylamine
    3. CAS NO:1092394-15-4
    4. Molecular Formula: C7H8N4O
    5. Molecular Weight: 164.16462
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1092394-15-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.48
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine(1092394-15-4)
    11. EPA Substance Registry System: 6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine(1092394-15-4)
  • 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: 1092394-15-4(Hazardous Substances Data)

1092394-15-4 Usage

Uses

Since the specific applications or uses of 6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine in various industries or scientific research have not been widely documented, it is not possible to provide a detailed list of its uses. However, given its chemical structure and belonging to the class of methoxytriazolopyridines, it may potentially be used in the following areas:
1. Used in Pharmaceutical Industry:
6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine could be used as a building block or intermediate in the synthesis of pharmaceutical compounds, given its unique chemical structure and potential reactivity.
2. Used in Chemical Research:
6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine may be utilized in chemical research to study its reactivity, stability, and potential interactions with other molecules, which could lead to the development of new chemical processes or materials.
3. Used in Material Science:
The unique structure of 6-Methoxy-[1,2,4]triazolo[1,5-a]pyridin-2-amine may offer specific properties that could be exploited in the development of new materials with tailored characteristics for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 1092394-15-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,2,3,9 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1092394-15:
(9*1)+(8*0)+(7*9)+(6*2)+(5*3)+(4*9)+(3*4)+(2*1)+(1*5)=154
154 % 10 = 4
So 1092394-15-4 is a valid CAS Registry Number.

1092394-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

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

1.2 Other means of identification

Product number -
Other names 6-methoxy[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:1092394-15-4 SDS

1092394-15-4Relevant articles and documents

Α 7 as intranuclear hydroxynicotinic acetylcholine receptor quinuclidines compd.

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, (2018/10/03)

PROBLEM TO BE SOLVED: To provide ligands for the nicotinic α-7 receptor used for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.SOLUTION: The disclosure provides compounds of the specified formula I, including their salts, and compositions and methods using the compounds.

QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS

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Page/Page column 130, (2011/05/11)

The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic 7 receptor and may be useful for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.

FUSED HETEROCYCLIC DERIVATIVES AND USE THEREOF

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, (2010/01/29)

The present invention provides a fused heterocyclic derivative having a strong kinase inhibitory activity and use thereof. The present invention relates to a compound represented by the formula wherein each symbol is as defined in the present specificatio

QUINUCLIDINE COMPOUNDS AS ALPHA-7 NICOTINIC ACETYLCHOLINE RECEPTOR LIGANDS

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Page/Page column 81, (2009/10/31)

The disclosure provides compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds are ligands for the nicotinic α7 receptor and may be useful for the treatment of various disorders of the central nervous system, especially affective and neurodegenerative disorders.

HETEROBICYCLIC COMPOUNDS AS KINASE INHIBITORS

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Page/Page column 184, (2009/01/24)

A compound represented by the formula (I): wherein Z1,Z2,Z3 and Z4 are the following combination, (Z1,Z2,Z3,Z4)=(CR4,N,CR5,C), (N,N,CR5,C), (N,C,CR5,N), (S,C,CR5,C) or (S,C,N,C); R1 and R2 are the same or different and each is (1) a hydrogen atom, (2) a halogen atom, (3) a group bonded via a carbon atom, (4) a group bonded via a nitrogen atom, (5) a group bonded via an oxygen atom or (6) a group bonded via a sulfur atom; R 3 is an amino optionally having substituent(s); R4 and R 5 are the same or different and each is (1) a hydrogen atom, (2) a halogen atom, (3) a group bonded via a carbon atom, (4) a group bonded via a nitrogen atom, (5) a group bonded via an oxygen atom or (6) a group bonded via a sulfur atom; R3 and R4 optionally form a ring optionally having substituent(s); and a group represented by the formula (A) is a cyclic group optionally having substituent(s), or a salt thereof

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