50434-36-1 Usage
Description
2-(4-nitrophenyl)acetyl chloride is an organic compound that consists of a 4-nitrophenyl group attached to an acetyl chloride moiety. It is a versatile reagent in organic synthesis and has unique chemical properties due to the presence of both the aromatic ring and the acetyl chloride functional group.
Uses
Used in Organic Synthesis:
2-(4-nitrophenyl)acetyl chloride is used as a reactant or starting material for the preparation of artificial receptors. Its reactivity and the presence of the nitro group make it a valuable building block in the synthesis of complex organic molecules, particularly those with potential applications in supramolecular chemistry and molecular recognition.
Used in Chemical Research:
In the field of chemical research, 2-(4-nitrophenyl)acetyl chloride is utilized as a reagent to study reaction mechanisms and to develop new synthetic methodologies. Its unique structure allows chemists to explore various reaction pathways and to gain insights into the fundamental aspects of organic chemistry.
Used in Pharmaceutical Industry:
2-(4-nitrophenyl)acetyl chloride is also used in the pharmaceutical industry as an intermediate in the synthesis of various drug candidates. Its ability to form stable acylating agents makes it suitable for the preparation of biologically active compounds with potential therapeutic applications.
Used in Material Science:
In material science, 2-(4-nitrophenyl)acetyl chloride can be employed in the development of new materials with specific properties. For instance, it can be used to create functional polymers or to modify the surface properties of materials for various applications, such as sensors, catalysts, or coatings.
Check Digit Verification of cas no
The CAS Registry Mumber 50434-36-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,4,3 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50434-36:
(7*5)+(6*0)+(5*4)+(4*3)+(3*4)+(2*3)+(1*6)=91
91 % 10 = 1
So 50434-36-1 is a valid CAS Registry Number.
InChI:InChI=1/C8H6ClNO3/c9-8(11)5-6-1-3-7(4-2-6)10(12)13/h1-4H,5H2
50434-36-1Relevant articles and documents
Reaction-based AIEE-active conjugated polymer as fluorescent turn on probe for mercury ions with good sensing performance
Shan, Yuanrong,Yao, Wenjie,Liang, Ziqin,Zhu, Lihong,Yang, Shuibin,Ruan, Zhijun
, p. 1 - 7 (2018)
Based on Hg2+-promoted deprotection reaction of thioketal, a type of thioketal decorated conjugated polymer (PTS) with the feature of aggregation induced emission enhancement (AIEE) was successfully synthesized as fluorescent turn on probe for
Quantitative activity-activity relationship (QAAR) driven design to develop hydroxamate derivatives of pentanoic acids as selective HDAC8 inhibitors: synthesis, biological evaluation and binding mode of interaction studies
Adhikari, Nilanjan,Amin, Sk. Abdul,Das, Sanjib,Ghosh, Balaram,Jha, Tarun,Routholla, Ganesh,Trivedi, Prakruti,Vijayasarathi, Dhanya
, p. 17149 - 17162 (2021/10/04)
Histone deacetylase 8 (HDAC8) has been implicated as a potential drug target of many diseases including cancer. HDAC8 isoform selectivity over other class-I HDACs is a major concern nowadays. In this work, a series of pentanoic acid based hydroxamates wit
Palladium-Catalyzed 2-(Neopentylsulfinyl)aniline Directed C–H Acetoxylation and Alkenylation of Arylacetamides
Barysevich, Maryia V.,Laktsevich-Iskryk, Marharyta V.,Krech, Anastasiya V.,Zhabinskii, Vladimir N.,Khripach, Vladimir A.,Hurski, Alaksiej L.
supporting information, p. 937 - 943 (2020/02/25)
The 2-(neopentylsulfinyl)aniline directing group that promotes rapid palladium-catalyzed C–H acetoxylation and alkenylation of arylacetamides has been developed. The acetoxylation reaches completion within only 40 min at 100 °C and leads to the bis-functionalized products. Alternatively, the reaction can be carried out at room temperature, which is beneficial for sensitive substrates. For the alkenylation, we have developed a protocol in which easily available 1-substituted cyclopropanols were employed as equivalents of vinyl ketones.