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2-Benzo[1,3]dioxol-5-ylmethyl-2H-pyrazol-3-ylamine is a complex organic compound with the molecular formula C11H10N2O2. It is characterized by a pyrazole ring fused with a benzodioxole ring, with an amino group attached to the pyrazole. This chemical is known for its potential applications in the synthesis of pharmaceuticals and agrochemicals due to its unique structure and reactivity. It can be used as an intermediate in the production of various compounds with biological activity, such as anti-inflammatory or antimicrobial agents. The compound's properties, such as its solubility and stability, can be influenced by the presence of functional groups and the overall molecular structure, making it a versatile building block in organic synthesis.

3528-55-0

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3528-55-0 Usage

Chemical structure

Pyrazole derivative with a benzodioxole group attached to the nitrogen atom

Potential applications

Pharmaceutical intermediate, synthesis of organic compounds, research tool in pharmaceutical and chemical industries

Potential biological activities

Presence of pyrazole and benzodioxole moieties may lead to important biological properties

Importance for further study and development

Compound may have potential for further research and development in various industries

Check Digit Verification of cas no

The CAS Registry Mumber 3528-55-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,2 and 8 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 3528-55:
(6*3)+(5*5)+(4*2)+(3*8)+(2*5)+(1*5)=90
90 % 10 = 0
So 3528-55-0 is a valid CAS Registry Number.

3528-55-0Upstream product

3528-55-0Downstream Products

3528-55-0Relevant academic research and scientific papers

TETRAZOLE COMPOUNDS AS OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 15, (2011/04/25)

The invention relates to tetrazole compounds of formula (I) wherein X, Y, Z, R1, R2 and R3 are as described in the description; to pharmaceutically acceptable salts thereof, and to the use of such compounds use as medicaments, especially as orexin receptor antagonists.

Approach to the library of fused pyridine-4-carboxylic acids by combes-type reaction of acyl pyruvates and electron-rich amino heterocycles

Volochnyuk, Dmitriy M.,Ryabukhin, Sergey V.,Plaskon, Andrey S.,Dmytriv, Yuri V.,Grygorenko, Oleksandr O.,Mykhailiuk, Pavel K.,Krotko, Dmitriy G.,Pushechnikov, Alexei,Tolmachev, Andrey A.

scheme or table, p. 510 - 517 (2010/09/05)

A library of fused pyridine-4-carboxylic acids (including pyrazolo[3,4-b]pyridines, isoxazolo[5,4-b]pyridines, furo[2,3-b]pyridines, thieno[2,3-b]pyridines, and pyrido[2,3-d]pyrimidines) was generated by Combes-type reaction of acyl pyruvates and electron-rich amino heterocycles followed by hydrolysis of the ester. The library members were also demonstrated to undergo the standard combinatorial transformations including amide coupling and esterification, as well as less common heterocyclizations to 1,2,4-triazoles and 1,2,4-oxadiazoles.

TETRAZOLE COMPOUNDS AS OREXIN RECEPTOR ANTAGONISTS

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Page/Page column 37, (2010/01/07)

The invention relates to tetrazole compounds of formula (I) wherein X, Y, Z, R1, R2 and R3 are as described in the description; to pharmaceutically acceptable salts thereof, and to the use of such compounds use as medicaments, especially as orexin receptor antagonists.

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