90674-24-1 Usage
Uses
Used in Organic Synthesis:
2-(thiophen-2-yl)pent-4-yn-2-ol is used as a key intermediate in the synthesis of various organic compounds. Its unique structure allows for the formation of new chemical bonds and the creation of novel molecules with potential applications in various industries.
Used in Research:
2-(thiophen-2-yl)pent-4-yn-2-ol is used as a research compound to study its chemical properties and potential applications. Researchers are interested in understanding how 2-(thiophen-2-yl)pent-4-yn-2-ol interacts with other molecules and how it can be used to develop new materials or drugs.
Used in Pharmaceutical Industry:
2-(thiophen-2-yl)pent-4-yn-2-ol is used as a potential building block for the development of new pharmaceuticals. Its unique structure may contribute to the creation of novel drugs with improved efficacy and reduced side effects.
Used in Agrochemical Industry:
2-(thiophen-2-yl)pent-4-yn-2-ol is used as a potential component in the development of new agrochemicals, such as pesticides or herbicides. Its unique properties may provide new ways to control pests and weeds in agriculture.
Used in Materials Science:
2-(thiophen-2-yl)pent-4-yn-2-ol is used as a potential component in the development of new materials with unique properties. Its incorporation into materials may lead to the creation of new materials with improved performance in various applications, such as electronics or energy storage.
Check Digit Verification of cas no
The CAS Registry Mumber 90674-24-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,7 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 90674-24:
(7*9)+(6*0)+(5*6)+(4*7)+(3*4)+(2*2)+(1*4)=141
141 % 10 = 1
So 90674-24-1 is a valid CAS Registry Number.
90674-24-1Relevant academic research and scientific papers
Zinc Amide Catalyzed Regioselective Allenylation and Propargylation of Ketones with Allenyl Boronate
Yamashita, Yasuhiro,Cui, Yi,Xie, Peizhong,Kobayashi, Shu
supporting information, p. 6042 - 6045 (2016/01/09)
Zinc amide catalyzed, regioselective allenylation and propargylation of ketones with allenyl boronate is reported. Tertiary allenyl and homopropargyl alcohols were obtained, respectively, in high selectivities, from the same starting materials, simply by changing the reaction conditions. The substrate scope was wide. Mechanistic studies suggest that the reactions are controlled under kinetic and thermodynamic conditions.
Asymmetric propargylation of ketones using allenylboronates catalyzed by chiral biphenols
Barnett, David S.,Schaus, Scott E.
supporting information; experimental part, p. 4020 - 4023 (2011/10/02)
Chiral biphenols catalyze the enantioselective asymmetric propargylation of ketones using allenylboronates. The reaction uses 10 mol % of 3,3′-Br2-BINOL as the catalyst and allenyldioxoborolane as the nucleophile, in the absence of solvent, and
