37920-25-5 Usage
Description
1-(4-Butylphenyl)ethan-1-one, also known as 4'-n-Butylacetophenone, is an organic compound that serves as a crucial intermediate in the synthesis of various chemicals and materials. It is characterized by its unique molecular structure, which features a butyl group attached to a phenyl ring, with an ethanone functional group at the end. This structure endows it with specific properties that make it suitable for a range of applications.
Uses
1. Used in the Chemical Synthesis Industry:
1-(4-Butylphenyl)ethan-1-one is used as an organic chemical synthesis intermediate for the production of various compounds. Its unique structure allows it to be a versatile building block in the synthesis of complex organic molecules, contributing to the development of new materials and chemicals with diverse applications.
2. Used in the Liquid Crystal Industry:
1-(4-Butylphenyl)ethan-1-one is also utilized as an intermediate in the production of liquid crystals. Liquid crystals are materials that exhibit properties between those of conventional liquids and solid crystals, making them highly valuable in the field of display technology. 1-(4-Butylphenyl)ethan-1-one's specific molecular structure plays a crucial role in the formation and stabilization of liquid crystal phases, enabling the development of advanced display technologies with improved performance characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 37920-25-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,7,9,2 and 0 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 37920-25:
(7*3)+(6*7)+(5*9)+(4*2)+(3*0)+(2*2)+(1*5)=125
125 % 10 = 5
So 37920-25-5 is a valid CAS Registry Number.
InChI:InChI=1/C12H16O/c1-3-4-5-11-6-8-12(9-7-11)10(2)13/h6-9H,3-5H2,1-2H3
37920-25-5Relevant articles and documents
Unprecedented nucleophilic addition of organolithiums to aromatic aldehydes and ketones by complexation with aluminum tris(2,6-diphenylphenoxide)
Maruoka, Keiji,Ito, Masahiro,Yamamoto, Hisashi
, p. 9091 - 9092 (1995)
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Design of Benzimidazolyl Phosphines Bearing AlterableP,OorP,N-Coordination: Synthesis, Characterization, and Insights into Their Reactivity
Wong, Shun Man,Choy, Pui Ying,Zhao, Qingyang,Yuen, On Ying,Yeung, Chung Chiu,So, Chau Ming,Kwong, Fuk Yee
supporting information, p. 2265 - 2271 (2021/05/05)
A new series of hemilabile benzimidazolyl phosphines is reported. Entities in this ligand family can be easily assembled and prepared on a large scale via a simple one-pot procedure. X-ray crystallographic analyses show that the Pd metal center can coordinate in different fashions, where it relies on the size of the ?PR2group. With the same ligand scaffold, the ligand having a ?PCy2moiety displays better efficiency in expediting aromatic C-C bond-coupling reactions, while the ligand associated with a ?P-t-Bu2group, in contrast, promotes C-N bond-forming reactions.
Generation of Alkyl Radical through Direct Excitation of Boracene-Based Alkylborate
Hashizume, Daisuke,Hosoya, Takamitsu,Nakamura, Kei,Ohmiya, Hirohisa,Sato, Yukiya,Sumida, Yuto
supporting information, p. 9938 - 9943 (2020/06/27)
The generation of tertiary, secondary, and primary alkyl radicals has been achieved by the direct visible-light excitation of a boracene-based alkylborate. This system is based on the photophysical properties of the organoboron molecule. The protocol is applicable to decyanoalkylation, Giese addition, and nickel-catalyzed carbon-carbon bond formations such as alkyl-aryl cross-coupling or vicinal alkylarylation of alkenes, enabling the introduction of various C(sp3) fragments to organic molecules.