51175-78-1 Usage
Uses
Used in Organic Synthesis:
(1-bromocyclobutyl)(phenyl)methanone is used as a reactive building block for the synthesis of various organic compounds. Its unique structure allows it to participate in a wide range of chemical reactions, making it a valuable component in the creation of new molecules.
Used in Pharmaceutical Production:
(1-bromocyclobutyl)(phenyl)methanone is used as a precursor in the production of pharmaceuticals. Its versatility and reactivity enable the development of new drugs with potential therapeutic benefits.
Used in Agrochemical Production:
(1-bromocyclobutyl)(phenyl)methanone is also used as a precursor in the production of agrochemicals. Its chemical properties make it suitable for the synthesis of compounds used in agriculture to protect crops and enhance yields.
Used in Industrial Chemical Production:
(1-bromocyclobutyl)(phenyl)methanone is utilized in the production of various industrial chemicals. Its ability to undergo multiple chemical reactions contributes to the development of a diverse range of chemical products for different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 51175-78-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,7 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 51175-78:
(7*5)+(6*1)+(5*1)+(4*7)+(3*5)+(2*7)+(1*8)=111
111 % 10 = 1
So 51175-78-1 is a valid CAS Registry Number.
51175-78-1Relevant academic research and scientific papers
Iron-Catalyzed Acyl Migration of Tertiary α-Azidyl Ketones: Synthetic Approach toward Enamides and Isoquinolones
Yang, Tonghao,Fan, Xing,Zhao, Xiaopeng,Yu, Wei
supporting information, p. 1875 - 1879 (2018/04/16)
This paper reports that tertiary α-azidyl phenyl ketones can be transformed into enamides by treatment with FeBr2 at elevated temperature in DMF. The reaction proceeds via 1,2-benzoyl migration from α-carbon to the nitrogen atom, accompanied by expulsion of a nitrogen molecule. This protocol is suitable for the synthesis of N-(cyclopent-1-en-1-yl)benzamides, N-(cyclohex-1-en-1-yl)benzamides, and N-benzoyl-α-methyl enamines and provides a convenient approach toward isoquinolones.
