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(4-nitrophenyl)(1H-pyrazol-5-yl)methanone is a chemical compound characterized by the molecular formula C10H7N3O3. It is a yellow solid that is prominently utilized in the realms of organic synthesis and medicinal chemistry. (4-nitrophenyl)(1H-pyrazol-5-yl)methanone is distinguished by the presence of a nitro group and a pyrazole ring, both of which are recognized for their wide-ranging biological activities. The integration of these functional groups renders (4-nitrophenyl)(1H-pyrazol-5-yl)methanone an indispensable building block in the development of novel pharmaceuticals and in the exploration of their interactions with biological systems. Furthermore, its distinctive structure and properties position it as a valuable asset in chemical research and drug discovery endeavors.

40711-96-4

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40711-96-4 Usage

Uses

Used in Organic Synthesis:
(4-nitrophenyl)(1H-pyrazol-5-yl)methanone is employed as a key intermediate in organic synthesis for the creation of various chemical compounds. Its unique structure, which includes a nitro group and a pyrazole ring, allows for a broad spectrum of reactions, making it a versatile component in the synthesis of a diverse array of molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, (4-nitrophenyl)(1H-pyrazol-5-yl)methanone is used as a building block for the development of new pharmaceuticals. (4-nitrophenyl)(1H-pyrazol-5-yl)methanone's functional groups, the nitro group and the pyrazole ring, are known for their biological activities, which can be harnessed to design drugs with specific therapeutic properties.
Used in Chemical Research:
(4-nitrophenyl)(1H-pyrazol-5-yl)methanone serves as a valuable tool in chemical research, particularly in the study of reaction mechanisms and the development of new synthetic methods. Its distinctive structure and properties make it an ideal candidate for probing the reactivity of various functional groups and for testing novel reaction conditions.
Used in Drug Discovery:
(4-nitrophenyl)(1H-pyrazol-5-yl)methanone is also utilized in drug discovery processes, where its unique structure and functional groups can be exploited to identify potential drug candidates with novel mechanisms of action. The study of (4-nitrophenyl)(1H-pyrazol-5-yl)methanone's interactions with biological systems can provide insights into the design of new therapeutic agents.
Used in Pharmaceutical Industry:
Within the pharmaceutical industry, (4-nitrophenyl)(1H-pyrazol-5-yl)methanone is used as a starting material or a synthetic intermediate for the production of various drugs. Its presence in the synthesis of pharmaceuticals highlights its importance in the development of new medications with improved efficacy and safety profiles.

Check Digit Verification of cas no

The CAS Registry Mumber 40711-96-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,7,1 and 1 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 40711-96:
(7*4)+(6*0)+(5*7)+(4*1)+(3*1)+(2*9)+(1*6)=94
94 % 10 = 4
So 40711-96-4 is a valid CAS Registry Number.

40711-96-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-nitrophenyl)-(1H-pyrazol-5-yl)methanone

1.2 Other means of identification

Product number -
Other names 3-p-Nitrobenzoylpyrazol

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:40711-96-4 SDS

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