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2,5-Dimethyl-4-phenyl-2H-pyrazol-3-ylamine is a chemical compound with the molecular formula C12H14N2. It is a derivative of pyrazole, a heterocyclic organic compound consisting of a five-membered aromatic ring with two nitrogen atoms and three carbon atoms. The compound features two methyl groups (CH3) at the 2nd and 5th positions and a phenyl group (C6H5) attached to the 4th position of the pyrazole ring. The amine group (-NH2) is present at the 3rd position, making it a potentially useful intermediate in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity.

3654-22-6

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3654-22-6 Usage

General Description

2,5-DIMETHYL-4-PHENYL-2H-PYRAZOL-3-YLAMINE is a chemical compound with the molecular formula C13H15N3. It is a pyrazole derivative with two methyl groups and a phenyl group attached to the pyrazole ring. This chemical is used in the synthesis of pharmaceuticals and agrochemicals, and it has been studied for its potential biological and pharmacological properties. Its structure suggests that it may act as a ligand for various receptors or enzymes, and it may exhibit biological activity as an inhibitor or stimulant. Further research is needed to fully understand the potential uses and effects of 2,5-DIMETHYL-4-PHENYL-2H-PYRAZOL-3-YLAMINE.

Check Digit Verification of cas no

The CAS Registry Mumber 3654-22-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,6,5 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3654-22:
(6*3)+(5*6)+(4*5)+(3*4)+(2*2)+(1*2)=86
86 % 10 = 6
So 3654-22-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H13N3/c1-8-10(11(12)14(2)13-8)9-6-4-3-5-7-9/h3-7H,12H2,1-2H3

3654-22-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,5-dimethyl-4-phenylpyrazol-3-amine

1.2 Other means of identification

Product number -
Other names 1,3-dimethyl-4-phenylpyrazol-5-ylamine

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:3654-22-6 SDS

3654-22-6Downstream Products

3654-22-6Relevant academic research and scientific papers

Catalytic system for inhibition of amination-type reaction and palladium-catalysed direct arylation using non-protected pyrazole derivatives

Derridj, Fazia,Roger, Julien,Djebbar, Safia,Doucet, Henri

experimental part, p. 747 - 750 (2012/04/23)

The palladium-catalysed direct arylation at C-4 of non-protected 5-aminopyrazoles was found to proceed in high yields using a variety of aryl bromides. The choice of potassium acetate as the base was found to be crucial to inhibit the amination reaction a

5-Aminopyrazoles from enolisable ketones and 1-cyano-1-alkylhydrazines

Ryckmans, Thomas,Viehe, Heinz-Gunter,Feneau-Dupont, Janine,Tinant, Bernard,Declercq, Jean-Paul

, p. 1729 - 1734 (2007/10/03)

The reaction of enolisable ketones with 1-alkyl-1-cyanohydrazines leads to the corresponding cyanohydrazones. These compounds cyclise under thermal or mildly basic conditions, furnishing the corresponding 5-aminopyrazoles in good yield. In some cases, the hydrazones cannot be isolated, and the pyrazole derivatives are directly obtained. Hydrazone-enehydrazine tautomerism was observed, but no subsequent [3,3] rearrangement.

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