480438-21-9 Usage
Uses
Used in Organic Synthesis:
BPGD is used as a catalyst for various organic reactions, including asymmetric synthesis of chiral compounds and polymerization reactions. Its high catalytic activity and selectivity make it a valuable tool in synthetic organic chemistry.
Used in Catalyst Industry:
BPGD is used as a catalyst in the Catalyst Industry, where it plays a crucial role in enhancing the efficiency and selectivity of various chemical reactions. Its ability to catalyze asymmetric synthesis and polymerization reactions contributes to the development of new materials and pharmaceuticals.
Used in Materials Science:
BPGD is used as a versatile building block in Materials Science for the development of new materials. Its unique properties and reactivity make it suitable for creating innovative materials with improved performance and functionality.
Used in Drug Discovery:
BPGD has shown potential as a valuable compound in Drug Discovery, where it can be utilized in the synthesis of pharmaceuticals and the development of new drugs. Its catalytic properties and ability to participate in various organic reactions contribute to the discovery of novel therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 480438-21-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,0,4,3 and 8 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 480438-21:
(8*4)+(7*8)+(6*0)+(5*4)+(4*3)+(3*8)+(2*2)+(1*1)=149
149 % 10 = 9
So 480438-21-9 is a valid CAS Registry Number.
InChI:InChI=1/C20H32B2O12/c1-9(2)27-17(23)13-14(18(24)28-10(3)4)32-21(31-13)22-33-15(19(25)29-11(5)6)16(34-22)20(26)30-12(7)8/h9-16H,1-8H3/t13-,14-,15-,16-/m0/s1
480438-21-9Relevant academic research and scientific papers
PREPARATION OF DIBORONIC ESTERS
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Page 17, (2008/06/13)
This invention relates to a process for the preparation of an ester of diboronic acid comprising reacting a tetrakis(dialkylamino)diboron with an alcohol to form the ester and a volatile dialkylamine, wherein the volatile dialkylamine is liberated from the reaction mixture in gaseous form.
Boronic compounds
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, (2008/06/13)
This invention relates to a diboron derivative of formula (I) or a diboron derivative of formula (II) or a diboron derivative of formula (III) where R1, R2, R3 and R4 are each independently selected from the group consisting of optionally substituted alkyl, optionally substituted alkenyl, optionally substituted aryl, optionally substituted cycloalkyl, optionally substituted cycloalkenyl, a group of the formula —(R5Q)mR6 where Q is selected from O, S, NR7, optionally substituted arylene and optionally substituted cycloalkylene, m is an integer selected from 1 to 3, the or and each R5 is independently an optionally substituted C1-C3 alkylene, R6 is C1-C3 alkyl or hydrogen, and R7 is hydrogen or C1-C12 alkyl; each X is independently selected from O, S(O)n and NR7, where n is an integer from 0 to 3, R7 is hydrogen or C1-C12 alkyl, or one or more of —NR1R7, —NR2R7, —NR3R7 and —NR4R7 represent an optionally substituted 5 or 6 membered heterocyclyl group,and A, A1 and A2 are divalent groups which may or may not be different.
