1260900-80-8 Usage
General Description
N-Ethyl-N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)ethanamine is a chemical compound that belongs to the group of organic compounds known as benzylamines. It is commonly used as a reagent in organic synthesis and chemical research. This chemical is also known for its applications in the pharmaceutical and agrochemical industries. Due to its unique structure and properties, N-Ethyl-N-(3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzyl)ethanamine can be used as a building block in the synthesis of various biologically active molecules and functional materials. Additionally, it can be utilized as a ligand in coordination chemistry and as a precursor in the production of fine chemicals and pharmaceuticals.
Check Digit Verification of cas no
The CAS Registry Mumber 1260900-80-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,6,0,9,0 and 0 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1260900-80:
(9*1)+(8*2)+(7*6)+(6*0)+(5*9)+(4*0)+(3*0)+(2*8)+(1*0)=128
128 % 10 = 8
So 1260900-80-8 is a valid CAS Registry Number.
1260900-80-8Relevant articles and documents
Microwave-mediated synthesis of an arylboronate library
Spencer, John,Baltus, Christine B.,Patel, Hiren,Press, Neil J.,Callear, Samantha K.,Male, Louise,Coles, Simon J.
experimental part, p. 24 - 31 (2011/04/15)
A series of arylboronates has been synthesized from the reaction of 2-(2-, (3-, or (4-(bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 1{1-3} respectively with a range of N-, S-, and O-nucleophiles, using microwave-mediated chemistry. For the synthesis of N- and S-substituted boronates, a supported base, PS-NMM, was employed, and many reactions were complete within 15 min. With O-nucleophiles, a mixture of tetrabutylammonium bromide, potassium carbonate, and sodium hydroxide was employed. The resulting aminomethyl, mercaptomethyl, or alkoxy-/phenoxymethyl-arylboronates were subjected to microwave-mediated Suzuki Miyaura coupling reactions to afford a range of biaryls in moderate to good yields. The X-ray structures of five boronates were determined.
