1203671-64-0 Usage
Description
5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-iMidazole is a boron-containing imidazole derivative with the molecular formula C11H16BNO2. It is characterized by a unique structure that features a boron atom attached to the imidazole ring, which endows the molecule with distinctive reactivity and properties. 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-iMidazole is a valuable building block in the synthesis of pharmaceuticals and agrochemicals, and it plays a significant role in various organic reactions.
Uses
Used in Organic Synthesis:
5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-iMidazole is used as a key intermediate in organic synthesis for the preparation of complex organic molecules. Its unique boron-containing structure allows for versatile reactivity, making it a preferred choice for the synthesis of a wide range of compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-iMidazole is used as a building block for the development of new drugs. Its special structural features and properties contribute to the creation of innovative therapeutic agents with improved efficacy and selectivity.
Used in Agrochemical Development:
5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-iMidazole is also utilized in the agrochemical sector as a precursor for the synthesis of novel agrochemicals. Its unique reactivity and properties enable the development of more effective and environmentally friendly pesticides and other agricultural chemicals.
Used in Suzuki-Miyaura Cross-Coupling Reactions:
In the field of organic chemistry, 5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-iMidazole is employed as a reactant in Suzuki-Miyaura cross-coupling reactions. This powerful synthetic method allows for the formation of carbon-carbon bonds, facilitating the construction of complex molecular architectures.
Used in Boron-Mediated Transformations:
5-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-1H-iMidazole is utilized in various boron-mediated transformations, which are essential for the synthesis of a diverse array of organic compounds. Its unique boron-containing structure enables these transformations, expanding the scope of synthetic methodologies available to chemists.
Check Digit Verification of cas no
The CAS Registry Mumber 1203671-64-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,3,6,7 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1203671-64:
(9*1)+(8*2)+(7*0)+(6*3)+(5*6)+(4*7)+(3*1)+(2*6)+(1*4)=120
120 % 10 = 0
So 1203671-64-0 is a valid CAS Registry Number.
1203671-64-0Relevant articles and documents
2-METHYL-QUINAZOLINES
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Page/Page column 285, (2018/10/19)
The present invention describes 2-methyl-quinazoline compounds of general formula (I), methods of preparing said compounds, intermediate compounds useful for preparing said compounds, pharmaceutical compositions and combinations comprising said compounds, and the use of said compounds for manufacturing pharmaceutical compositions. The 2-methyl substituted quinazoline compounds of general formula(I) effectively and selectively inhibit the Ras-Sos interaction without significantly targeting the EGFR receptor. They are therefore useful for the treatment or prophylaxis of diseases, in particular of hyperproliferative disorders, such as cancer as a sole agent or in combination with other active ingredients.
