380430-70-6 Usage
General Description
(4-tert-butoxycarboxyphenyl)boronic acid is a boronic acid compound with the chemical formula C11H15BO4. It is a white solid that is sparingly soluble in water. This chemical is often used as a building block in the synthesis of pharmaceuticals and other organic compounds. Boronic acids are known for their ability to form stable complexes with diols and other Lewis bases, making them useful reagents in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. The (4-tert-butoxycarboxyphenyl)boronic acid is an important reagent in the field of medicinal chemistry and drug discovery for the development of new medications.
Check Digit Verification of cas no
The CAS Registry Mumber 380430-70-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,0,4,3 and 0 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 380430-70:
(8*3)+(7*8)+(6*0)+(5*4)+(4*3)+(3*0)+(2*7)+(1*0)=126
126 % 10 = 6
So 380430-70-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H15BO5/c1-11(2,3)17-10(13)16-9-6-4-8(5-7-9)12(14)15/h4-7,14-15H,1-3H3
380430-70-6Relevant articles and documents
An easy route to (hetero)arylboronic acids
Erb, William,Hellal, Akila,Albini, Mathieu,Rouden, Jacques,Blanchet, Jerome
, p. 6608 - 6612 (2014/06/09)
An unprecedented spontaneous reactivity between diazonium salts and diboronic acid has been unveiled, leading to a versatile arylboronic acid synthesis directly from (hetero)arylamines. This fast reaction (35 min overall) tolerates a wide range of functional groups and is carried out under very mild conditions. The radical nature of the reaction mechanism has been investigated.
