105869-43-0 Usage
General Description
2-(Cyclohexylethyl)boronic acid is a chemical compound that belongs to the class of organic compounds known as boronic acids and derivatives. These substances are compounds containing a boronic acid or its derivative, which is characterized by a boron atom bonded to an oxygen atom and two carbon atoms. It is used in chemical synthesis and in the development of a variety of pharmaceuticals as a boronic acid derivative. 2-(cyclohexylethyl)boronic acid is known for its distinct properties such as high stability and reactivity that make it suitable for chemical coupling reactions. It is generally sold in its solid form and should be handled with care due to its corrosive nature.
Check Digit Verification of cas no
The CAS Registry Mumber 105869-43-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,8,6 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 105869-43:
(8*1)+(7*0)+(6*5)+(5*8)+(4*6)+(3*9)+(2*4)+(1*3)=140
140 % 10 = 0
So 105869-43-0 is a valid CAS Registry Number.
InChI:InChI=1/C8H17BO2/c10-9(11)7-6-8-4-2-1-3-5-8/h8,10-11H,1-7H2
105869-43-0Relevant articles and documents
Visible-Light-Mediated Aerobic Oxidation of Organoboron Compounds Using in Situ Generated Hydrogen Peroxide
Weng, Wei-Zhi,Liang, Hao,Zhang, Bo
, p. 4979 - 4983 (2018)
A simple and general visible-light-mediated oxidation of organoboron compounds has been developed with rose bengal as the photocatalyst, substoichiometric Et3N as the electron donor, as well as air as the oxidant. This mild and metal-free protocol shows a broad substrate scope and provides a wide range of aliphatic alcohols and phenols in moderate to excellent yields. Notably, the robustness of this method is demonstrated on the stereospecific aerobic oxidation of organoboron compounds.
