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25288-75-9

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25288-75-9 Usage

Description

(1E,4E)-1,5-Bis(4-nitrophenyl)penta-1,4-dien-3-one is a yellow, crystalline solid that features two 4-nitrophenyl groups attached to a penta-1,4-diene-3-one molecule. This chemical compound is utilized in organic synthesis and chemical research, serving as a starting material for the preparation of a variety of compounds, such as pharmaceuticals and agrochemicals. It has demonstrated significant anti-inflammatory and anticancer properties, which makes it a valuable asset for studying the biological activities of similar compounds. Moreover, its chemical structure is advantageous for the synthesis of more complex organic molecules. However, due to its classification as a hazardous substance, it is crucial to handle this compound with care, using proper personal protective equipment and working in a well-ventilated area.

Uses

Used in Organic Synthesis:
(1E,4E)-1,5-Bis(4-nitrophenyl)penta-1,4-dien-3-one is used as a starting material in organic synthesis for the preparation of various compounds, including pharmaceuticals and agrochemicals. Its unique structure allows for the creation of a wide range of molecules with potential applications in different fields.
Used in Chemical Research:
In the realm of chemical research, (1E,4E)-1,5-Bis(4-nitrophenyl)penta-1,4-dien-3-one is used as a valuable tool for studying the biological activities of similar compounds. Its anti-inflammatory and anticancer properties make it an important subject for research aimed at understanding and developing new therapeutic agents.
Used in Pharmaceutical Development:
(1E,4E)-1,5-Bis(4-nitrophenyl)penta-1,4-dien-3-one is used as an intermediate in the synthesis of pharmaceuticals. Its chemical properties and structure contribute to the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Production:
(1E,4E)-1,5-Bis(4-nitrophenyl)penta-1,4-dien-3-one is also used in agrochemical production, where it serves as a starting material for the synthesis of various agrochemicals that can be used in agriculture to protect crops and enhance yields.
Used in the Synthesis of Complex Organic Molecules:
Due to its chemical structure, (1E,4E)-1,5-Bis(4-nitrophenyl)penta-1,4-dien-3-one is used as an intermediate for the synthesis of more complex organic molecules, which can have a range of applications in various industries, including materials science and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 25288-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,2,8 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25288-75:
(7*2)+(6*5)+(5*2)+(4*8)+(3*8)+(2*7)+(1*5)=129
129 % 10 = 9
So 25288-75-9 is a valid CAS Registry Number.

25288-75-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name (1E,4E)-1,5-Bis(4-nitrophenyl)penta-1,4-dien-3-one

1.2 Other means of identification

Product number -
Other names 1,4-Pentadien-3-one, 1,5-bis(4-nitrophenyl)-

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:25288-75-9 SDS

25288-75-9Relevant articles and documents

Cu(OAc)2/TFA-promoted formal [3 + 3] cycloaddition/oxidation of enamines and enones for synthesis of multisubstituted aromatic amines

Li, Liang,Zhao, Mi-Na,Ren, Zhi-Hui,Li, Jian-Li,Guan, Zheng-Hui

supporting information; experimental part, p. 3506 - 3509 (2012/08/08)

New strategies for the oxidative cycloaddition of enones with enamines are developed. These cycloaddition reactions directly afford substituted aromatic amines, which are important in organic chemistry, in moderate to good yield. Cu(OAc)2/TFA is shown to be essential to achieve high reaction efficiency.

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