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Methyl 4-phenyl-1H-pyrazole-3-carboxylate is a chemical compound characterized by the molecular formula C12H11N3O2. It is a white to light yellow solid that plays a significant role in the field of organic chemistry. This versatile compound is widely recognized for its use as a reagent in the synthesis of a variety of pharmaceuticals, agrochemicals, and other organic compounds. Its ability to serve as a building block in the creation of biologically active molecules underscores its importance in chemical research and development.

5932-28-5

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5932-28-5 Usage

Uses

Used in Organic Chemistry:
Methyl 4-phenyl-1H-pyrazole-3-carboxylate is used as a reagent for the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds, leveraging its structural properties to facilitate the creation of a broad range of chemical entities.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, Methyl 4-phenyl-1H-pyrazole-3-carboxylate is used as an intermediate in the preparation of pyrazole derivatives. These derivatives have been studied for their potential therapeutic applications, including antitumor, antimicrobial, and anti-inflammatory properties, making Methyl 4-phenyl-1H-pyrazole-3-carboxylate a valuable asset in drug discovery and development.
Used in Agrochemical Development:
Similarly, in agrochemicals, Methyl 4-phenyl-1H-pyrazole-3-carboxylate serves as a key intermediate, contributing to the development of new compounds designed to protect crops and enhance agricultural productivity.
Used in Chemical Research and Development:
Methyl 4-phenyl-1H-pyrazole-3-carboxylate is also used in the development of new materials and chemical processes, where its unique properties allow for innovation and advancement in various chemical applications, solidifying its importance in the broader field of chemical research and development.

Check Digit Verification of cas no

The CAS Registry Mumber 5932-28-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,9,3 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5932-28:
(6*5)+(5*9)+(4*3)+(3*2)+(2*2)+(1*8)=105
105 % 10 = 5
So 5932-28-5 is a valid CAS Registry Number.
InChI:InChI=1/C19H21N3O4/c1-26-18-4-2-3-15(13-18)14-20-9-11-21(12-10-20)19(23)16-5-7-17(8-6-16)22(24)25/h2-8,13H,9-12,14H2,1H3

5932-28-5SDS

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 [4-[(3-methoxyphenyl)methyl]piperazin-1-yl]-(4-nitrophenyl)methanone

1.2 Other means of identification

Product number -
Other names 4-Phenyl-1(2)H-pyrazol-3-carbonsaeure-methylester

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:5932-28-5 SDS

5932-28-5Relevant academic research and scientific papers

AMINOPYRIMIDINE COMPOUND USED FOR INHIBITING ACTIVITY OF PROTEIN KINASE

-

Paragraph 0158; 0160, (2021/10/02)

The present invention relates to an aminopyrimidine compound having an inhibitory effect on the activity of protein kinase as well as the preparation and use thereof. Specifically, disclosed by the present invention is an aminopyrimidine compound represented by formula (I), or a pharmaceutically acceptable salt, stereoisomer, solvate or hydrate thereof, as well as a pharmaceutical composition comprising said compound and a use method therefor. The method comprises a method for treating cell proliferative diseases and conditions such as cancer and immune diseases.

Preparations of 4-substituted 3-carboxypyrazoles

Janin, Yves L.

, p. 1410 - 1414 (2014/01/06)

The scopes of three synthetic methods reported for the preparation of an array of 3-pyrazolecarboxylates featuring substituents on position 4 were investigated. The first one is based on the potassium permanganate oxidation of methylpyrazoles. The second starts with the condensation between DMF dimethylacetal and ethyl pyruvate and is followed by the addition of hydrazine hydrochloride. The last one makes use of the cycloaddition of diazomethane on acrylate esters followed by a bromine-based oxidative rearrangement into 4-substituted 3-pyrazole esters.

NEW EFFICIENT SYNTHESIS OF 3(5)-CARBOMETHOXY-4-ARYLPYRAZOLES FROM 3-ARYL-2,3-DEHYDROAMINO ACID DERIVATIVES

Catiela, Carlos,Villegas, M. Dolores Diaz de,Gainza, M. Pilar

, p. 165 - 172 (2007/10/02)

3(5)-Carbomethoxy-4-arylpyrazoles can be easily obtained by aromatization with boron trifluoride etherate of 4-aryl-3-acetamido(or benzamido)-3-carbomethoxy-Δ1-pyrazolines synthesized by 1,3-dipolar cycloaddition of diazomethane with 3-aryl-2,3

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