501944-42-9 Usage
Uses
Used in Organic Synthesis:
5-Fluorobenzothiophene-2-boronic acid is used as a building block in organic synthesis for the preparation of various biologically active molecules. Its unique structure allows for the creation of a wide range of compounds with potential applications in medicine, agriculture, and other fields.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Fluorobenzothiophene-2-boronic acid is used as a key intermediate in the synthesis of drugs with therapeutic properties. Its ability to form carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions enables the development of complex molecular structures with desired pharmacological activities.
Used in Agrochemical Industry:
5-Fluorobenzothiophene-2-boronic acid is also utilized in the agrochemical industry for the synthesis of pesticides and other crop protection agents. Its reactivity and structural diversity contribute to the development of effective and environmentally friendly agrochemicals.
Used as a Reagent in Suzuki-Miyaura Cross-Coupling Reactions:
5-Fluorobenzothiophene-2-boronic acid is commonly used as a reagent in Suzuki-Miyaura cross-coupling reactions, a widely employed method for the formation of carbon-carbon bonds in organic synthesis. This reaction allows chemists to efficiently construct complex organic compounds with high selectivity and under mild conditions, facilitating the synthesis of a variety of target molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 501944-42-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,9,4 and 4 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 501944-42:
(8*5)+(7*0)+(6*1)+(5*9)+(4*4)+(3*4)+(2*4)+(1*2)=129
129 % 10 = 9
So 501944-42-9 is a valid CAS Registry Number.
InChI:InChI=1/C8H6BFO2S/c10-6-1-2-7-5(3-6)4-8(13-7)9(11)12/h1-4,11-12H
501944-42-9Relevant articles and documents
C-benzo five-membered heteroaromatic aryl glucoside derivative as well as preparation method and application thereof
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Paragraph 0063; 0064, (2016/10/08)
The invention discloses a C-benzo five-membered heteroaromatic aryl glucoside derivative shown in the general formula (I) (in the description), a preparation method of the derivative or an intermediate of the derivative, as well as application of the derivative. In the general formula (I), R, R1, R2, R3, R4, X and Y are defined in the description. The C-benzo five-membered heteroaromatic aryl glucoside derivative is novel in structure, has quite strong inhibitory activity on SGLT-2, has high selection ratio for SGLT-1 and SGLT-2, and can be used for preparing drugs for treating and preventing diseases relevant to SGLT-2.
