61676-61-7 Usage
Uses
Used in Chemical Synthesis:
2-Isopropoxy-4,4,6-trimethyl-[1,3,2]dioxaborinane is used as a coupling reagent for facilitating the formation of carbon-carbon and carbon-heteroatom bonds in organic synthesis. Its ability to promote the formation of these bonds makes it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Palladium-Catalyzed Cross-Coupling Reactions:
In the field of organic chemistry, 2-Isopropoxy-4,4,6-trimethyl-[1,3,2]dioxaborinane is used as a coupling reagent in palladium-catalyzed cross-coupling reactions. These reactions are essential for the formation of new chemical bonds between different organic molecules, allowing for the creation of a wide range of complex organic compounds with potential applications in various industries.
Used in Pharmaceutical Industry:
2-Isopropoxy-4,4,6-trimethyl-[1,3,2]dioxaborinane is used as a key intermediate in the synthesis of various pharmaceutical compounds. Its ability to facilitate the formation of essential chemical bonds makes it a crucial component in the development of new drugs and therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 2-Isopropoxy-4,4,6-trimethyl-[1,3,2]dioxaborinane is used as a coupling reagent for the synthesis of various agrochemicals, such as pesticides and herbicides. Its role in the formation of complex organic molecules contributes to the development of more effective and targeted agrochemical products.
Overall, 2-Isopropoxy-4,4,6-trimethyl-[1,3,2]dioxaborinane is a versatile and valuable compound in the fields of chemical synthesis, pharmaceuticals, and agrochemicals, playing a crucial role in the development of new and innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 61676-61-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,1,6,7 and 6 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 61676-61:
(7*6)+(6*1)+(5*6)+(4*7)+(3*6)+(2*6)+(1*1)=137
137 % 10 = 7
So 61676-61-7 is a valid CAS Registry Number.
61676-61-7Relevant articles and documents
Noncryogenic preparation of functionalized arylboronic esters through a magnesium-iodine exchange with in situ quench
Demory, Emilien,Blandin, Veronique,Einhorn, Jacques,Chavant, Pierre Y.
experimental part, p. 710 - 716 (2012/10/23)
Various functionalized aryl boronic esters derived from hexylene glycol and pinacol were prepared in excellent yields according to a simple, safe procedure. The metal-halogen exchange reaction between iPrMgCl? LiCl and aryl iodides is performed
2-Isopropoxy-borolane, -borinane and -borole Complexes of N,N'-Ethylenebis(salicylaldimine)
Tripathi, S. M.,Singh, R. V.,Tandon, J. P.
, p. 90 - 93 (2007/10/02)
Reactions of unsymmetrical monoisopropoxyboranes with N,N'-ethylenebis(salicylaldimine) (Salen H2) in different molar ratios lead to the formation of (ZO2)B(Salen H2) and (ZO2)B(Salen)B(ZO2) type of derivatives.Similar reactions of boric acid in acetic anhydride medium have resulted in the isolation of (OAc)2B(Salen H) and (OAc)2B(Salen)B(OAc)2 type of compounds.These have been characterized on the basis of elemental analysis, conductance and molecular weight data.The infrared, electronic and proton magnetic resonance spectra of some of the representative derivatives have also been studied.
