501014-47-7 Usage
General Description
2-(1,3-Dioxolan-2-on-4-yl)-1-ethylboronic acid pinacol ester is a chemical compound with the molecular formula C10H17BO4. It is a boronic acid ester derivative, which is commonly used as a building block in organic synthesis. 2-(1,3-DIOXOLAN-2-ON-4-YL)-1-ETHYLBORONIC ACID PINACOL ESTER is known for its ability to form boronate complexes with various electrophiles, making it a valuable reagent for cross-coupling reactions in organic chemistry. It also has potential applications in the pharmaceutical industry, as boronic acid esters have been studied for their biological activity and use in drug development.
Check Digit Verification of cas no
The CAS Registry Mumber 501014-47-7 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 7 respectively.
Calculate Digit Verification of CAS Registry Number 501014-47:
(8*5)+(7*0)+(6*1)+(5*0)+(4*1)+(3*4)+(2*4)+(1*7)=77
77 % 10 = 7
So 501014-47-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H19BO5/c1-10(2)11(3,4)17-12(16-10)6-5-8-7-14-9(13)15-8/h8H,5-7H2,1-4H3
501014-47-7Relevant articles and documents
Process for preparing bisallylboranes and nonaromatic boronic acids
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, (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).
