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5-M-TOLYL-2H-PYRAZOL-3-YLAMINE is a chemical compound that belongs to the class of aromatic heterocyclic compounds. It is composed of a pyrazole ring with a 5-methyltolyl substituent and an amine group. This versatile compound has potential applications in various fields, including pharmaceuticals, agrochemicals, and materials science, making it a valuable asset in chemical research and industrial applications.

80568-96-3

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80568-96-3 Usage

Uses

Used in Pharmaceutical Industry:
5-M-TOLYL-2H-PYRAZOL-3-YLAMINE is used as a building block in the synthesis of biologically active compounds for pharmaceutical drugs. Its unique structure allows for the development of new drugs with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical field, 5-M-TOLYL-2H-PYRAZOL-3-YLAMINE is used as a building block in the synthesis of biologically active compounds for pesticides. Its incorporation into pesticide formulations can enhance their effectiveness in controlling pests and diseases in agriculture.
Used in Materials Science:
5-M-TOLYL-2H-PYRAZOL-3-YLAMINE has utility as a precursor in the preparation of advanced materials. Its unique chemical properties can contribute to the development of new materials with improved performance characteristics for various applications.
Used as a Ligand in Metal Coordination Chemistry:
5-M-TOLYL-2H-PYRAZOL-3-YLAMINE may also be used as a ligand in metal coordination chemistry. Its ability to form stable complexes with metal ions can be exploited in the design of new catalysts, sensors, and other functional materials.

Check Digit Verification of cas no

The CAS Registry Mumber 80568-96-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,6 and 8 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80568-96:
(7*8)+(6*0)+(5*5)+(4*6)+(3*8)+(2*9)+(1*6)=153
153 % 10 = 3
So 80568-96-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3/c1-7-3-2-4-8(5-7)9-6-10(11)13-12-9/h2-6H,1H3,(H3,11,12,13)

80568-96-3 Well-known Company Product Price

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  • Aldrich

  • (JRD0002)  3-m-Tolyl-1H-pyrazol-5-amine  AldrichCPR

  • 80568-96-3

  • JRD0002-1G

  • 1,611.09CNY

  • Detail

  • Aldrich

  • (CDS006521)  3-m-Tolyl-1H-pyrazol-5-amine  AldrichCPR

  • 80568-96-3

  • CDS006521-50MG

  • 644.67CNY

  • Detail

80568-96-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-(3-methylphenyl)-1H-pyrazol-3-amine

1.2 Other means of identification

Product number -
Other names 3-m-tolyl-1h-pyrazol-5-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:80568-96-3 SDS

80568-96-3Downstream Products

80568-96-3Relevant academic research and scientific papers

Polysubstituted heterocyclic derivative, preparation method thereof and application of polysubstituted heterocyclic derivative in medicine

-

Paragraph 0035-0037; 0053; 0057-0058; 0351; 0355-0356, (2021/06/02)

The invention provides a polysubstituted heterocyclic derivative, a preparation method thereof and application of the polysubstituted heterocyclic derivative in medicine, and belongs to the technical field of medicinal chemistry. The polysubstituted heterocyclic derivative is a compound shown in a general formula I or II, a pharmaceutically acceptable salt or a solvate of the compound, and the compound can inhibit mRNA demethylase on the protease level and is used for treating diseases related to mRNA demethylase functions.

A new, one-pot, multicomponent synthesis of 5-aza-9-deaza-adenines under microwave irradiation

Lim, Felicia Phei Lin,Luna, Giuseppe,Dolzhenko, Anton V.

, p. 5159 - 5163 (2014/12/10)

A new, practical, three-component method for the synthesis of 5-aza-9-deaza-adenines is developed. Aminopyrazoles react in a one-pot fashion with triethyl orthoformate and cyanamide under microwave irradiation affording 5-aza-9-deaza-adenines in good yiel

Novel potent neuropeptide Y Y5 receptor antagonists: Synthesis and structure-activity relationships of phenylpiperazine derivatives

Takahashi, Toshiyuki,Sakuraba, Aya,Hirohashi, Tomoko,Shibata, Takunobu,Hirose, Masaaki,Haga, Yuji,Nonoshita, Katsumasa,Kanno, Tetsuya,Ito, Junko,Iwaasa, Hisashi,Kanatani, Akio,Fukami, Takehiro,Sato, Nagaaki

, p. 7501 - 7511 (2007/10/03)

A series of phenylpiperazine derivatives were synthesized and evaluated for their neuropeptide Y (NPY) Y5 receptor antagonistic activities. The benzindane portion of 2 was replaced by 1-phenylpiperazine, resulting in novel urea derivative 3f. Subsequent optimization of the phenylpiperazine template by substitution of the phenyl moiety resulted in a series of (2-methanesulfonamidephenyl)piperazine derivatives that showed potent binding affinity and antagonistic activity for the Y5 receptor.

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