1073338-97-2 Usage
Description
2-(4-bromo-3,5-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a complex organic compound that features a boron atom bonded to a dioxaborolane ring and a substituted phenyl group. 2-(4-bromo-3,5-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is characterized by its bromine atom at the para position and methyl groups at the ortho and meta positions on the phenyl ring. It is a versatile reagent in organic chemistry, particularly in the field of medicinal chemistry and materials science.
Uses
Used in Organic Synthesis:
2-(4-bromo-3,5-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a reactant in organic synthesis for the creation of various complex molecules and pharmaceutical compounds. Its unique structure allows for selective functionalization and the formation of new carbon-carbon and carbon-heteroatom bonds, which are crucial in the development of novel drugs and advanced materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-(4-bromo-3,5-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is used as a building block for the synthesis of bioactive molecules. Its bromine atom can be replaced with other functional groups, enabling the development of new drugs with improved pharmacological properties, such as enhanced potency, selectivity, and reduced side effects.
Used in Materials Science:
2-(4-bromo-3,5-dimethylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is also utilized in materials science for the development of advanced materials with specific properties. Its ability to form stable bonds with other molecules allows for the creation of materials with tailored characteristics, such as improved mechanical strength, thermal stability, and chemical resistance.
Check Digit Verification of cas no
The CAS Registry Mumber 1073338-97-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,7,3,3,3 and 8 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1073338-97:
(9*1)+(8*0)+(7*7)+(6*3)+(5*3)+(4*3)+(3*8)+(2*9)+(1*7)=152
152 % 10 = 2
So 1073338-97-2 is a valid CAS Registry Number.
1073338-97-2Relevant articles and documents
D-π-A triarylboron compounds with tunable push-pull character achieved by modification of both the donor and acceptor moieties
Zhang, Zuolun,Edkins, Robert M.,Nitsch, J?rn,Fucke, Katharina,Eichhorn, Antonius,Steffen, Andreas,Marder, Todd B.,Wang, Yue
, p. 177 - 190 (2015)
The push-pull character of a series of donor-bithienyl-acceptor compounds has been tuned by adopting triphenylamine or 1,1,7,7-tetramethyljulolidine as a donor and B(2,6-Me2-4-RC6H2)2 (R=Me, C6F5 or 3
NEW INDANYLOXYDIHYDROBENZOFURANYLACETIC ACIDS
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Paragraph 0863, (2013/10/07)
The present invention relates to compounds of general formula I, wherein the groups R1, R2 and m are defined as in claim 1, which have valuable pharmacological properties, in particular bind to the GPR40 receptor and modulate its activity. The compounds are suitable for treatment and prevention of diseases which can be influenced by this receptor, such as metabolic diseases, in particular diabetes type 2.