501014-42-2 Usage
Uses
Used in Pharmaceutical Industry:
CIS-STILBENEBORONIC ACID DIETHANOLAMINE ESTER is used as a reagent in the synthesis of new drugs, leveraging its ability to form stable complexes with organic molecules, which aids in the development of innovative pharmaceutical compounds.
Used in Material Science:
In the field of material science, CIS-STILBENEBORONIC ACID DIETHANOLAMINE ESTER is used as a component in the creation of functional materials and advanced materials, taking advantage of its complex-forming properties to enhance material properties.
Used in Catalysis:
CIS-STILBENEBORONIC ACID DIETHANOLAMINE ESTER is utilized as a catalyst or in the development of catalytic systems, capitalizing on its chemical properties to improve reaction efficiency and selectivity in various chemical processes.
Used as a Fluorescent Probe in Biotechnology:
In biotechnology, CIS-STILBENEBORONIC ACID DIETHANOLAMINE ESTER is used as a fluorescent probe for the detection and imaging of biological molecules, given its potential to bind with specific biomolecules and fluoresce upon interaction, thereby aiding in research and diagnostics.
Check Digit Verification of cas no
The CAS Registry Mumber 501014-42-2 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 501014-42:
(8*5)+(7*0)+(6*1)+(5*0)+(4*1)+(3*4)+(2*4)+(1*2)=72
72 % 10 = 2
So 501014-42-2 is a valid CAS Registry Number.
InChI:InChI=1/C18H20BNO2/c1-3-7-16(8-4-1)15-18(17-9-5-2-6-10-17)19-21-13-11-20-12-14-22-19/h1-10,15,20H,11-14H2/b18-15+
501014-42-2Relevant 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).
