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2-(3-oxonon-1-en-1-yl)phenyl 4-nitrobenzoate is a chemical compound characterized by the molecular formula C22H20N2O6. It is a derivative of 4-nitrobenzoic acid, featuring a benzene ring with a 2-(3-oxonon-1-en-1-yl)phenyl group attached to it. 2-(3-oxonon-1-en-1-yl)phenyl 4-nitrobenzoate is distinguished by its unique molecular structure and chemical properties, which render it a valuable and versatile building block in the fields of organic synthesis, pharmaceutical research, drug development, material science, and biological studies.

69232-93-5

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69232-93-5 Usage

Uses

Used in Organic Synthesis:
2-(3-oxonon-1-en-1-yl)phenyl 4-nitrobenzoate is utilized as a key intermediate in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for multiple points of reactivity, facilitating the synthesis of a wide range of compounds with diverse applications.
Used in Pharmaceutical Research:
In pharmaceutical research, 2-(3-oxonon-1-en-1-yl)phenyl 4-nitrobenzoate serves as a precursor for the development of new drugs. Its chemical properties make it suitable for the synthesis of bioactive molecules with potential therapeutic effects.
Used in Drug Development:
2-(3-oxonon-1-en-1-yl)phenyl 4-nitrobenzoate is employed as a building block in drug development, where its structural features can be leveraged to design and optimize pharmaceutical agents with improved efficacy, selectivity, and safety profiles.
Used in Material Science:
In material science, 2-(3-oxonon-1-en-1-yl)phenyl 4-nitrobenzoate is used for the development of novel materials with specific properties. Its molecular structure can contribute to the creation of materials with tailored characteristics for various applications, such as sensors, catalysts, or advanced materials with unique mechanical, electrical, or optical properties.
Used in Biological Studies:
2-(3-oxonon-1-en-1-yl)phenyl 4-nitrobenzoate is also utilized in biological studies, where it can be employed to investigate the interactions between small molecules and biological targets, such as enzymes, receptors, or other proteins. This can lead to a better understanding of biological processes and the discovery of new bioactive compounds with potential applications in medicine and biotechnology.

Check Digit Verification of cas no

The CAS Registry Mumber 69232-93-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,9,2,3 and 2 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 69232-93:
(7*6)+(6*9)+(5*2)+(4*3)+(3*2)+(2*9)+(1*3)=145
145 % 10 = 5
So 69232-93-5 is a valid CAS Registry Number.

69232-93-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [2-[(E)-3-oxonon-1-enyl]phenyl] 4-nitrobenzoate

1.2 Other means of identification

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Other names -

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

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More Details:69232-93-5 SDS

69232-93-5Upstream product

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