135615-38-2 Usage
Explanation
The compound is named based on its constituent parts, which include 1,3,2-dioxaborolane and a biphenyl derivative.
Explanation
The compound is made up of two distinct parts, each with its own unique properties and uses.
Explanation
The first component of the compound is a boron-containing organic compound, which is often used as a reagent in organic synthesis.
Explanation
The second component of the compound is a biphenyl derivative, which is commonly used in the production of organic materials and as a building block for the synthesis of various compounds.
5. Versatile Chemical Compound
Explanation
The combination of the two components results in a versatile chemical compound that can be used in a wide range of applications.
Explanation
Due to its versatility, the compound has uses in various fields, including the development of pharmaceuticals, agrochemicals, and materials for scientific research and development.
Explanation
The 1,3,2-dioxaborolane component of the compound is commonly used as a reagent in organic synthesis, which is a key process in the production of many different types of chemicals.
Explanation
The biphenyl derivative component of the compound is often used as a building block for the synthesis of various compounds, making it a valuable tool in the field of chemistry.
Explanation
The biphenyl derivative component is also often utilized in the production of organic materials, which are used in a wide range of applications, from pharmaceuticals to plastics.
Constituent Components
1,3,2-Dioxaborolane and 2,2'-[1,1'-biphenyl]-4,4'-diylbis-
Boron-Containing
1,3,2-Dioxaborolane
Biphenyl Derivative
2,2'-[1,1'-biphenyl]-4,4'-diylbis-
Applications
Pharmaceuticals, Agrochemicals, and Material Science
Organic Synthesis
Used as a Reagent
Building Block
For the Synthesis of Various Compounds
Organic Material Production
Utilized in the Production of Organic Materials
Check Digit Verification of cas no
The CAS Registry Mumber 135615-38-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,6,1 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 135615-38:
(8*1)+(7*3)+(6*5)+(5*6)+(4*1)+(3*5)+(2*3)+(1*8)=122
122 % 10 = 2
So 135615-38-2 is a valid CAS Registry Number.
135615-38-2Relevant academic research and scientific papers
Michels, Jasper J.,O'Connell, Michael J.,Taylor, Peter N.,Wilson, Joanne S.,Cacialli, Franco,Anderson, Harry L.
, p. 6167 - 6176 (2003)
A series of conjugated polyrotaxane insulated molecular wires are synthesised by aqueous Suzuki polymerisation, using hydrophobic binding to promote threading of the cyclodextrin units. These polyrotaxanes have conjugated polymer cores based on poly(para-
Synthesis and complexation of back-to-back capped bis-dioxocyclams
Gil, Jun Mo,David, Scott,Reiff, Angela L.,Hegedus, Louis S.
, p. 5858 - 5865 (2008/10/09)
Pyridine-capped 5,12-dioxocyclams were coupled back-to-back directly, with one or two intervening phenyl groups, an ethynyl group, or a diazo group via Suzuki, Sonogashira, or reductive coupling of the 4-nitropyridine monocyclam. These bis-dioxocyclams linked through extended π-conjugated systems were complexed to copper(II) and cobalt-(III), producing bis-metal complexes which were characterized spectroscopically and electrochemically. These studies gave little evidence for electronic communication between metal centers across the π-conjugated linkers.
Efficient and convenient nonaqueous workup procedure for the preparation of arylboronic esters
Wong, Ken-Tsung,Chien, Yuh-Yih,Liao, Yuan-Li,Lin, Chang-Chih,Chou, Meng-Yen,Leung, Man-Kit
, p. 1041 - 1044 (2007/10/03)
An efficient one-pot synthetic protocol for the synthesis of arylboronic esters has been established. The concentrated addition mixture of trimethylborate with aryl Grignard reagents was treated with low molecular weight diols (ethylene glycol, 1,3-propandiol) and toluene, the corresponding arylboronic esters were isolated in a convenient way with high yields. The diols not only serve as water replacement for the workup step, but also as well as the reagent for the preparation of arylboronic esters.
