950511-16-7 Usage
Description
1-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene is a complex heterocyclic chemical compound that features a naphthalene ring fused to a 1,3,2-diazaborinyl ring, and a benzene ring attached to a 1,3,2-dioxaborolan-2-yl group. 1-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, with its unique structure containing both boron and carbon atoms, is utilized in various organic synthesis reactions and serves as a key building block in the development of advanced materials, including polymers and pharmaceuticals. Its distinctive molecular architecture lends itself to the creation of innovative molecular structures with potential applications in material science and medicinal chemistry.
Uses
Used in Organic Synthesis:
1-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene is used as an intermediate in organic synthesis for the creation of complex molecular structures. Its unique fusion of rings and functional groups allows for a wide range of chemical reactions, facilitating the synthesis of novel compounds with diverse properties.
Used in Material Science:
In the field of material science, 1-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene is used as a building block for the development of advanced materials. Its incorporation into polymers and other materials can enhance their properties, such as strength, stability, and reactivity, making them suitable for various applications, including electronics, aerospace, and automotive industries.
Used in Pharmaceutical Industry:
1-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene is used as a key component in the production of pharmaceuticals. Its unique structure allows for the design of new drugs with improved efficacy and selectivity, potentially leading to the development of novel therapeutic agents for the treatment of various diseases and medical conditions.
Used in Research and Development:
This complex chemical compound is also utilized in research and development settings, where it can be employed to study the properties and behavior of novel molecular structures. Its use in this context can contribute to the advancement of scientific knowledge and the discovery of new applications in various fields, including chemistry, biology, and engineering.
Check Digit Verification of cas no
The CAS Registry Mumber 950511-16-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,0,5,1 and 1 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 950511-16:
(8*9)+(7*5)+(6*0)+(5*5)+(4*1)+(3*1)+(2*1)+(1*6)=147
147 % 10 = 7
So 950511-16-7 is a valid CAS Registry Number.
950511-16-7Relevant articles and documents
The method for producing the phenyl boronic acid ester
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Paragraph 0113; 0114, (2018/09/26)
PROBLEM TO BE SOLVED: To provide a method for producing phenylboronic acid esters in good yield from diborons and aryl halides by using a nickel catalyst and a base. SOLUTION: In the method for producing phenylboronic acid esters represented by general formula (3), wherein A is an ethylene group or the like which may be substituted by a methyl group, R1is a fluorine atom or the like, and m is an integer of 0-5; diborons and a chlorobenzene derivative are reacted with each other by using a trimethylphosphine coordinated nickel catalyst and alkoxides. COPYRIGHT: (C)2013,JPOandINPIT
NiCl2(PMe3)2-catalyzed borylation of aryl chlorides
Yamamoto, Tetsuya,Morita, Tomoyuki,Takagi, Jun,Yamakawa, Tetsu
supporting information; experimental part, p. 5766 - 5769 (2012/01/06)
The cross-coupling of aryl chlorides and bis(pinacolato)diboron was achieved using NiCl2(PMe3)2 catalyst in the presence of metal 2,2,2-trifluoroethoxide. The catalyst smoothly provided the desired products regardless of a variety of functional groups and substituted positions.
Differentially protected benzenediboronic acids: Divalent cross-coupling modules for the efficient synthesis of boron-substituted oligoarenes
Noguchi, Hiroyoshi,Shioda, Takayuki,Chou, Chih-Ming,Suginome, Michinori
, p. 377 - 380 (2008/09/19)
On the basis of the boron-masking strategy, new divalent cross-coupling modules have been designed for the efficient synthesis of boronsubstituted oligoarenes. The modules, i.e., monoprotected o-, m-, and p-benzenediboronic acid derivatives, undergo highly selective SuzukiMiyaura coupling with sp 2 iodides, bromides, chlorides, and triflates, affording coupling products in which the protected boronyl groups are left intact.
