1201566-80-4 Usage
Description
Methyl 4,5-dimethoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is a chemical compound characterized by the molecular formula C18H25BO6. It is a boronic ester, which is a class of compounds known for their stability and selective reactivity. This makes it a valuable building block in the synthesis of various complex molecules, including pharmaceuticals, agrochemicals, and materials. Its versatility in forming carbon-carbon bonds is particularly noteworthy, and it is also used as a precursor in the preparation of biologically active compounds.
Uses
Used in Organic Synthesis:
Methyl 4,5-dimethoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is used as a reagent in organic synthesis for the formation of carbon-carbon bonds. Its selective reactivity and stability make it a valuable tool in the construction of complex molecular structures.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, Methyl 4,5-dimethoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is used as a building block in the synthesis of various drugs. Its role in creating carbon-carbon bonds is crucial for the development of new medicinal compounds.
Used in Agrochemical Synthesis:
Methyl 4,5-dimethoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is also employed in the synthesis of agrochemicals, contributing to the development of new pesticides and other agricultural products.
Used in Material Science:
In the field of material science, Methyl 4,5-dimethoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate is used as a precursor in the preparation of advanced materials with specific properties, such as improved strength or chemical resistance.
Safety Considerations:
It is important to handle Methyl 4,5-dimethoxy-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoate with care, as boronic esters can be toxic. Proper safety measures, including the use of a well-ventilated area and appropriate protective equipment, should be taken to minimize health risks during its use in chemical synthesis.
Check Digit Verification of cas no
The CAS Registry Mumber 1201566-80-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,5,6 and 6 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1201566-80:
(9*1)+(8*2)+(7*0)+(6*1)+(5*5)+(4*6)+(3*6)+(2*8)+(1*0)=114
114 % 10 = 4
So 1201566-80-4 is a valid CAS Registry Number.
1201566-80-4Relevant articles and documents
Synthesis and biological evaluation of N-substituted benzo[c] phenanthrolines and benzo[c]phenanthrolinones as antiproliferative agents
Genès, Constance,Lenglet, Ga?lle,Depauw, Sabine,Nhili, Raja,Prado, Soizic,David-Cordonnier, Marie-Hélène,Michel, Sylvie,Tillequin, Fran?ois,Porée, Fran?ois-Hugues
scheme or table, p. 2117 - 2131 (2011/06/21)
Benzo[c]phenanthrolines and benzo[c]phenanthrolinones substituted by dialkylaminoalkyl side chains at position N5 and C6, respectively, were synthesised and their biological activity evaluated. They displayed interessant cytotoxicity associated with some DNA interactions. However, the low topoisomerase 1 affinity suggests that other cellular targets are responsible for the antiproliferative activity.
