62729-39-9 Usage
General Description
4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)BENZOIC ACID is a chemical compound that belongs to the family of benzoic acids. It is a white crystalline solid that is used in various industrial and research applications. 4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)BENZOIC ACID is commonly utilized in the synthesis of pharmaceuticals, agrochemicals, and materials science. It has also been studied for its potential as an anti-inflammatory agent and as a building block in organic chemistry reactions. The unique structure of 4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)BENZOIC ACID makes it a valuable tool for developing new chemical compounds with diverse properties and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 62729-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,2 and 9 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 62729-39:
(7*6)+(6*2)+(5*7)+(4*2)+(3*9)+(2*3)+(1*9)=139
139 % 10 = 9
So 62729-39-9 is a valid CAS Registry Number.
InChI:InChI=1/C12H15BO4/c1-12(2)7-16-13(17-8-12)10-5-3-9(4-6-10)11(14)15/h3-6H,7-8H2,1-2H3,(H,14,15)
62729-39-9Relevant articles and documents
Palladium-catalyzed synthesis of aromatic carboxylic acids with silacarboxylic acids
Friis, Stig D.,Andersen, Thomas L.,Skrydstrup, Troels
supporting information, p. 1378 - 1381 (2013/04/24)
Aryl iodides and bromides were easily converted to their corresponding aromatic carboxylic acids via a Pd-catalyzed carbonylation reaction using silacarboxylic acids as an in situ source of carbon monoxide. The reaction conditions were compatible with a wide range of functional groups, and with the aryl iodides, the carbonylation was complete within minutes. The method was adapted to the double and selective isotope labeling of tamibarotene.
