62729-39-9 Usage
Uses
Used in Pharmaceutical Synthesis:
4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)BENZOIC ACID is used as a key intermediate in the synthesis of pharmaceuticals. Its unique structure allows for the development of new chemical compounds with diverse properties and potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, 4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)BENZOIC ACID is used as a building block for the synthesis of various agrochemicals. Its versatility in chemical reactions enables the creation of new compounds with potential applications in agriculture.
Used in Materials Science:
4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)BENZOIC ACID is utilized in materials science for the development of new materials with unique properties. Its chemical structure contributes to the creation of innovative materials for various applications.
Used in Organic Chemistry Reactions:
As a building block in organic chemistry, 4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)BENZOIC ACID is used in various chemical reactions to synthesize new compounds with different properties. Its reactivity and structural features make it a valuable component in organic synthesis.
Used in Anti-Inflammatory Research:
4-(5,5-DIMETHYL-1,3,2-DIOXABORINAN-2-YL)BENZOIC ACID has been studied for its potential as an anti-inflammatory agent. Its unique structure may contribute to the development of new anti-inflammatory drugs with improved efficacy and reduced side effects.
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 academic research and scientific papers
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.
Halogen-magnesium exchange on unprotected aromatic and heteroaromatic carboxylic acids
Kopp, Felix,Wunderlich, Stefan,Knochel, Paul
, p. 2075 - 2077 (2008/02/09)
The magnesiation of halogenated aromatic and heteroaromatic carboxylic acids is accomplished by their treatment with MeMgCl in the presence of LiCl and subsequent reaction with i-PrMgCl·LiCl; the resulting double-magnesiated species react with a variety of electrophiles in up to 97% yield. The Royal Society of Chemistry.
