31915-26-1 Usage
Description
3-(2-Fluorophenyl)-3-oxopropionitrile, also known as 2-Fluorobenzoylacetonitrile (CAS# 31915-26-1), is an organic compound characterized by its yellow solid appearance. It is primarily recognized for its utility in various organic synthesis processes, making it a valuable component in the chemical industry.
Uses
Used in Organic Synthesis:
3-(2-Fluorophenyl)-3-oxopropionitrile is used as a synthetic building block for the creation of more complex organic molecules. Its unique structure, which includes a fluorophenyl group and a cyano group, allows it to participate in a range of chemical reactions, facilitating the synthesis of various compounds with different applications across multiple industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(2-Fluorophenyl)-3-oxopropionitrile is utilized as an intermediate in the development of new drugs. Its reactivity and structural diversity make it a promising candidate for the synthesis of novel pharmaceutical compounds, potentially leading to the discovery of new treatments for various diseases and medical conditions.
Used in Chemical Research:
3-(2-Fluorophenyl)-3-oxopropionitrile also plays a significant role in chemical research, where it is employed to study the properties and behavior of fluorinated organic compounds. Researchers use this compound to gain insights into the effects of fluorination on molecular interactions, reactivity, and stability, which can be applied to the design of new materials and chemicals with improved performance characteristics.
Used in Material Science:
In the field of material science, 3-(2-Fluorophenyl)-3-oxopropionitrile is used as a precursor for the development of advanced materials with specific properties. Its incorporation into polymers and other materials can lead to enhanced characteristics such as increased thermal stability, improved mechanical strength, or altered electronic properties, depending on the desired application.
Overall, 3-(2-Fluorophenyl)-3-oxopropionitrile is a versatile compound with a wide range of applications across various industries, including organic synthesis, pharmaceuticals, chemical research, and material science. Its unique chemical properties and reactivity make it a valuable asset in the development of new compounds, materials, and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 31915-26-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,9,1 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 31915-26:
(7*3)+(6*1)+(5*9)+(4*1)+(3*5)+(2*2)+(1*6)=101
101 % 10 = 1
So 31915-26-1 is a valid CAS Registry Number.
InChI:InChI=1/C9H6FNO/c10-8-4-2-1-3-7(8)9(12)5-6-11/h1-4H,5H2
31915-26-1Relevant articles and documents
Selective Synthesis of β-Ketonitriles via Catalytic Carbopalladation of Dinitriles
Zeng, Ge,Liu, Jichao,Shao, Yinlin,Zhang, Fangjun,Chen, Zhongyan,Lv, Ningning,Chen, Jiuxi,Li, Renhao
, p. 861 - 867 (2021/01/09)
A practical, convenient, and highly selective method of synthesizing β-ketonitriles from the Pd-catalyzed addition of organoboron reagents to dinitriles has been developed. This method provides excellent functional-group tolerance, a broad scope of substrates, and the convenience of using commercially available substrates. The method is expected to show further utility in future synthetic procedures.
Copper-catalyzed Aerobic Oxidative coupling of Aromatic Alcohols and Acetonitrile to β-Ketonitriles
Shen, Jiaxuan,Yang, Dejun,Liu, Yuxiao,Qin, Shuangshuang,Zhang, Jingwu,Sun, Jiangkai,Liu, Chunhui,Liu, Chaoyang,Zhao, Xiaomei,Chu, Changhu,Liu, Renhua
supporting information, p. 350 - 353 (2014/04/03)
A practical, convenient, and cheap coppercatalyzed aerobic oxidative coupling of aromatic alcohols and acetonitrile to β-ketonitriles has been developed. The green C-C bond formation involving the loss of two hydrogen atoms from the corresponding two carbons, respectively, unlocks opportunities for markedly different synthetic strategies.
Cascade synthesis of 3-aza-bicyclo[3.1.0]hex-2-ene derivatives from N-allyl enamines
Zhai, Sheng-Xian,Dong, Hong-Ru,Chen, Zi-Bao,Hu, Yi-Ming,Dong, Heng-Shan
, p. 8405 - 8412 (2015/03/04)
An efficient iodine-mediated cascade synthesis of 3-aza-bicyclo[3.1.0]hex-2-ene derivatives from easily prepared N-allyl enamines has been developed. The advantages of the reaction include facilitative preparation of substrates 3a-t, good functional group tolerance and transition-metal-free conditions.
