62707-11-3 Usage
Boron-containing heterocyclic compound
This compound contains a boron atom within a heterocyclic ring structure, which is a ring containing at least one non-carbon atom.
Common use in organic synthesis and material science
1H-Borole, 1-chloro-2,3,4,5-tetraphenylis frequently used as a building block or intermediate in the synthesis of various organic and inorganic compounds, as well as in the development of new materials.
Chloro-substituted tetraphenylborole
The presence of a chlorine atom in the compound's structure makes it a derivative of tetraphenylborole, which can be further functionalized or used in coordination chemistry.
Potential applications in coordination chemistry
The compound can form coordination complexes with metal ions, which can be used to study the properties and reactivity of the metal centers or as functional materials.
Use as a building block for functional materials
Due to its unique structure and reactivity, 1H-Borole, 1-chloro-2,3,4,5-tetraphenylcan be used to synthesize materials with specific properties, such as chemical sensors, molecular switches, and pharmaceutical compounds.
Versatile synthesis
The compound's structure and reactivity make it a valuable building block for the synthesis of a wide range of organic and inorganic compounds, allowing for the development of new chemical and material applications.
Check Digit Verification of cas no
The CAS Registry Mumber 62707-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,7,0 and 7 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 62707-11:
(7*6)+(6*2)+(5*7)+(4*0)+(3*7)+(2*1)+(1*1)=113
113 % 10 = 3
So 62707-11-3 is a valid CAS Registry Number.
62707-11-3Relevant articles and documents
Direct functionalization at the boron center of antiaromatic chloroborole
Braunschweig, Holger,Kupfer, Thomas
supporting information; experimental part, p. 4487 - 4489 (2009/05/06)
The presence of a reactive B-Cl bond allowed for the direct functionalization of the boron center in antiaromatic chloroborole ClBC 4Ph4, thus allowing for a selective fine tuning of the optical properties of borole derivatives and facilitating a potential new approach toward the introduction of borole moieties into the backbone of organic π-conjugated frameworks. The Royal Society of Chemistry.
