501014-44-4 Usage
Uses
Used in Pharmaceutical Industry:
2-Indanylboronic acid diethanolamine ester is used as a building block for the production of pharmaceuticals. Its ability to form carbon-carbon and carbon-heteroatom bonds makes it a valuable component in the synthesis of various drug molecules.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Indanylboronic acid diethanolamine ester is used as a precursor for the synthesis of agrochemicals. Its versatility in forming different types of chemical bonds allows for the creation of a wide range of agrochemical products.
Used in Fine Chemicals Industry:
2-Indanylboronic acid diethanolamine ester is used as a building block for the production of fine chemicals. Its ability to form carbon-carbon and carbon-heteroatom bonds makes it a valuable component in the synthesis of various specialty chemicals.
Used in Electronic Devices Industry:
2-Indanylboronic acid diethanolamine ester has potential applications in the development of materials for electronic devices. Its unique chemical properties can be utilized to create advanced materials with improved performance characteristics.
Used in Advanced Technologies Industry:
In the advanced technologies industry, 2-Indanylboronic acid diethanolamine ester can be used in the development of new materials for various applications. Its versatility and ability to form different types of chemical bonds make it a promising candidate for use in cutting-edge technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 501014-44-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,1,0,1 and 4 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 501014-44:
(8*5)+(7*0)+(6*1)+(5*0)+(4*1)+(3*4)+(2*4)+(1*4)=74
74 % 10 = 4
So 501014-44-4 is a valid CAS Registry Number.
InChI:InChI=1/C13H18BNO2/c1-2-4-12-10-13(9-11(12)3-1)14-16-7-5-15-6-8-17-14/h1-4,13,15H,5-10H2
501014-44-4Relevant academic research and scientific papers
Di(isopropylprenyl)borane: A new hydroboration reagent for the synthesis of alkyl and alkenyl boronic acids
Kalinin, Alexey V.,Scherer, Stefan,Snieckus, Victor
, p. 3399 - 3404 (2007/10/03)
The best of the old: The new hydroboration reagent 1 combines the selectivity of disiamylborane (2) with the reactivity towards carbonyls of allyl boranes 3. Conventional oxidative workup conditions are avoided, as facile hydrolysis in protic media provides the corresponding boronic acids with up to 99% anti-Markovnikov selectivities. A one-pot hydroboration/ Suzuki-Miyaura protocol adds to the synthetic value of 1.
Process for preparing bisallylboranes and nonaromatic boronic acids
-
, (2008/06/13)
A process for preparing bisallylboranes of the formula (I) by reacting a diene with sodium borohydride in the presence of an oxidant in an inert solvent, with the borane generated in situ reacting selectively with the diene to form the bis(allyl)borane of the formula (I) and the substituents R1 to R6 having the following meanings: R1-R6 are H, aryl or substituted or unsubstituted C1-C4-alkyl or two radicals R may be closed to form a cyclic system. As oxidant, it is possible to use, for example, alkyl halides or dialkyl sulfates. In a particularly preferred embodiment, the diene used is 2,5-dimethylhexa-2,4-diene (R1, R2, R5, R6=methyl, R3, R4=H).
