Welcome to LookChem.com Sign In|Join Free

CAS

  • or

66000-39-3

1-(4-CHLORO-PHENYL)-1H-PYRAZOL-3-YLAMINE is a chemical compound characterized by a pyrazole ring system with a 4-chlorophenyl substituent. It is a member of the aminopyrazole class, known for its diverse pharmaceutical and biological activities. 1-(4-CHLORO-PHENYL)-1H-PYRAZOL-3-YLAMINE is recognized for its potential as a building block in the synthesis of other organic compounds, particularly in the development of new drugs. Its unique structure and reactivity make it a valuable asset in the fields of medicinal chemistry and drug discovery, as well as in various chemical reactions and synthetic processes.

66000-39-3 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 66000-39-3 Structure

  • Basic information

    1. Product Name: 1-(4-CHLORO-PHENYL)-1H-PYRAZOL-3-YLAMINE
    2. Synonyms: 1-(4-CHLORO-PHENYL)-1H-PYRAZOL-3-YLAMINE;3-AMino-1-(4-chlorophenyl)-1H-pyrazole, 95%
    3. CAS NO:66000-39-3
    4. Molecular Formula: C9H8ClN3
    5. Molecular Weight: 193.63292
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 66000-39-3.mol

  • Chemical Properties

    1. Melting Point: 107-108℃
    2. Boiling Point: 349.04 °C at 760 mmHg
    3. Flash Point: 164.894 °C
    4. Appearance: /
    5. Density: 1.364 g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.66
    8. Storage Temp.: 2-8°C
    9. Solubility: N/A
    10. CAS DataBase Reference: 1-(4-CHLORO-PHENYL)-1H-PYRAZOL-3-YLAMINE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 1-(4-CHLORO-PHENYL)-1H-PYRAZOL-3-YLAMINE(66000-39-3)
    12. EPA Substance Registry System: 1-(4-CHLORO-PHENYL)-1H-PYRAZOL-3-YLAMINE(66000-39-3)

  • 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: 66000-39-3(Hazardous Substances Data)

66000-39-3 Usage

Uses

Used in Pharmaceutical Industry:
1-(4-CHLORO-PHENYL)-1H-PYRAZOL-3-YLAMINE is used as a building block for the synthesis of new drugs due to its diverse pharmaceutical and biological activities. Its unique structure and reactivity contribute to the development of innovative therapeutic agents.
Used in Medicinal Chemistry Research:
1-(4-CHLORO-PHENYL)-1H-PYRAZOL-3-YLAMINE is used as a research compound in medicinal chemistry to explore its potential applications and properties. Its presence in the aminopyrazole class makes it a promising candidate for further investigation and development.
Used in Chemical Reactions and Synthetic Processes:
1-(4-CHLORO-PHENYL)-1H-PYRAZOL-3-YLAMINE is used as a reagent in various chemical reactions and synthetic processes. Its structure and reactivity make it a valuable component in the creation of new organic compounds and materials.

Check Digit Verification of cas no

The CAS Registry Mumber 66000-39-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,0,0 and 0 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 66000-39:
(7*6)+(6*6)+(5*0)+(4*0)+(3*0)+(2*3)+(1*9)=93
93 % 10 = 3
So 66000-39-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8ClN3/c10-7-1-3-8(4-2-7)13-6-5-9(11)12-13/h1-6H,(H2,11,12)

66000-39-3 Well-known Company Product Price

  • Brand
  • (Code)Product description
  • CAS number
  • Packaging
  • Price
  • Detail

  • Alfa Aesar

  • (H32252)  3-Amino-1-(4-chlorophenyl)-1H-pyrazole, 95%   

  • 66000-39-3

  • 250mg

  • 2352.0CNY

  • Detail

66000-39-3SDS

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 1-(4-chlorophenyl)pyrazol-3-amine

1.2 Other means of identification

Product number -
Other names 1-(4-chlorphenyl)-1H-pyrazol-3-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:66000-39-3 SDS

66000-39-3Relevant articles and documents

1,3-SUBSTITUED PYRAZOLE COMPOUNDS USEFUL FOR REDUCTION OF VERY LONG CHAIN FATTY ACIC LEVELS

-

Paragraph 260, (2018/06/30)

Disclosed are chemical entities which are compounds of Formula (I) and pharmaceutically acceptable salts thereof, wherein Formula (I) has the structure: R1a, R1b, R2, R3, R4a, R4b and Y are as defined herein. These chemical entities are useful for reduction of very long chain fatty acid levels. These chemical entities and pharmaceutically acceptable compositions comprising such chemical entities can be useful for treating various diseases, disorders and conditions, such as adrenoleukodystrophy (ALD).

Copper(I)/Copper(II)-Assisted Tandem Catalysis: The Case Study of Ullmann/Chan-Evans-Lam N1,N3-Diarylation of 3-Aminopyrazole

Beyer, Astrid,Castanheiro, Thomas,Busca, Patricia,Prestat, Guillaume

, p. 2433 - 2436 (2015/08/24)

Unprecedented CuI/CuII-assisted tandem catalysis allowing an Ullmann/Chan-Evans-Lam sequence was achieved. This three-component, one-pot reaction triggered by a change in the oxidation state of the metal leads to the selective N1,N3-diarylation of 3-aminopyrazole. This new method should be a valuable tool for small-molecule drug discovery that requires suitable regio- and/or chemoselective strategies for the N-arylation of nitrogen-containing heterocycles. Tandem power: The first assisted tandem copper-catalyzed process, triggered by a change in the oxidation state of the metal, is developed to allow a one-pot Ullman/Chan-Evans-Lam sequence leading to the selective N1,N3-diarylation of 3-aminopyrazole.

QUINAZOLINEDIONE DERIVATIVES AS TRPA1 MODULATORS

-

Page/Page column 12-13, (2010/01/31)

The present invention provides Quinazolinedione derivatives as TRPA (Transient Receptor Potential subfamily A) modulators. In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by T

PROCESS FOR MAKING PYRAZOLE COMPOUNDS

-

Page 65, (2008/06/13)

This invention relates to a process for making pyrazole compoundsof formula I.

Process for preparing 1-phenyl-3-aminopyrazoles

-

, (2008/06/13)

1-PHENYL-3-AMINO-2-PYRAZOLINES ARE CATALYTICALLY OXIDIZED TO 1-PHENYL-3-AMINOPYRAZOLES, USING OXYGEN AND/OR AIR AS THE OXIDIZING AGENT AND IN THE PRESENCE OF COPPER SALTS, OPTIONALLY ASSOCIATED WITH METALLIC COPPER AND/OR AN AROMATIC, HETEROCYCLIC ORGANIC

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 66000-39-3