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CAS

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21203-83-8

2-phenoxypyridin-4-amine is a pyridine derivative with the molecular formula C11H9N3O, featuring a phenolic group at the 2-position and an amino group at the 4-position of the pyridine ring. This chemical compound exhibits structural and biological activities, making it a promising candidate for pharmaceutical and agrochemical applications.

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  • 21203-83-8 Structure

  • Basic information

    1. Product Name: 2-phenoxypyridin-4-amine
    2. Synonyms: 2-phenoxypyridin-4-amine
    3. CAS NO:21203-83-8
    4. Molecular Formula: C11H10N2O
    5. Molecular Weight: 186.2099
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 21203-83-8.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.: Keep in dark place,Inert atmosphere,Room temperature
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-phenoxypyridin-4-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-phenoxypyridin-4-amine(21203-83-8)
    11. EPA Substance Registry System: 2-phenoxypyridin-4-amine(21203-83-8)

  • 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: 21203-83-8(Hazardous Substances Data)

21203-83-8 Usage

Uses

Used in Pharmaceutical Industry:
2-phenoxypyridin-4-amine is used as a potential drug candidate for its anti-inflammatory and analgesic properties, offering a new avenue for the development of therapeutic agents.
Used in Agrochemical Industry:
2-phenoxypyridin-4-amine is used as a building block for the synthesis of novel organic compounds with diverse biological activities, contributing to the discovery of new agrochemicals with improved efficacy and safety.
Used in Chemical Synthesis:
2-phenoxypyridin-4-amine is used as a key intermediate in the synthesis of various organic compounds, enabling the creation of a wide range of molecules with potential applications in different fields of science and technology.
Researchers are actively exploring the potential uses and properties of 2-phenoxypyridin-4-amine, aiming to unlock its full potential in various industries and scientific domains.

Check Digit Verification of cas no

The CAS Registry Mumber 21203-83-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,0 and 3 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21203-83:
(7*2)+(6*1)+(5*2)+(4*0)+(3*3)+(2*8)+(1*3)=58
58 % 10 = 8
So 21203-83-8 is a valid CAS Registry Number.

21203-83-8SDS

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 2-phenoxypyridin-4-amine

1.2 Other means of identification

Product number -
Other names 4-amino-2-phenoxypyridine

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:21203-83-8 SDS

21203-83-8Downstream Products

21203-83-8Relevant articles and documents

N-pyridine-4-yl-benzamide Cdc37 inhibitor as well as derivative and application thereof

-

Paragraph 0099-0102, (2021/05/19)

The invention discloses an N-pyridine-4-yl-benzamide Cdc37 inhibitor with a structure as shown in a general formula (I) as well as a derivative and application thereof. The compound disclosed by the invention can inhibit Cdc37 protein and downstream custo

ON THE BIPYRIDYL FORMATION IN REACTIONS OF 2-CHLOROPYRIDINE DERIVATIVES WITH POTASSIUM AMIDE IN LIQUID AMMONIA

Streef, Johannis W.,Plas, Henk C. van der,Harkema, Sybolt

, p. 2313 - 2325 (2007/10/02)

In the reaction of 2,6-dichloropyridine and 2,6-dichloro-3-phenylpyridine with potassium amide in liquid ammonia at -70 deg C, formation of derivatives of 4,4'-bipyridyl and 3,4'-bipyridyl is observed.The 4,4' coupling products are far in excess to the 3,4' coupling products.When the reaction is carried out at -70 deg C in the presence of potassium permanganate, the corresponding 4-aminopyridines are the main products. 2-Chloro-6-phenoxypyridine is very unreactive with this aminating reagent at -70 deg C as well as -33 deg C, but in the presence of potassium permanganate at -33 deg C 4-amino-2-chloro-6-phenoxypyridine is formed in fair yield.The mechanisms of the formation of the bipyridyls and 4-aminopyridines are presented.

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