950511-16-7

Basic information

• Product Name: 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
• Synonyms: 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
• CAS NO: 950511-16-7
• Molecular Weight: 370.067
• Mol File: 950511-16-7.mol

Chemical Properties

• CAS DataBase Reference: 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(CAS DataBase Reference)
• NIST Chemistry Reference: 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(950511-16-7)
• EPA Substance Registry System: 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(950511-16-7)

Safety Data

• Hazardous Substances Data: 950511-16-7(Hazardous Substances Data)

Usage

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.

Upstream product

• 927384-44-9 2-(4-bromophenyl)-2,3-dihydro-1H-naphtho[1,8-de] [1,3,2]diazaborinine 
• 73183-34-3 bis(pinacol)diborane 
• 5467-74-3 4-Bromophenylboronic acid 
• 479-27-6 naphthalene-1,8-diamine 
• 1336918-65-0 2-(4-chlorophenyl)-2,3-dihydro-1H-naphtho[1,8-de] [1,3,2]diazaborinine 

Downstream Products

• 950511-27-0 4-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-(2-thiophenyl)benzene 
• 950511-26-9 4-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-(2-pyridyl)benzene 
• 950511-21-4 4-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4'-nitro-1,1'-biphenyl 
• 950511-20-3 2-([1,1'-biphenyl]-4-yl)-2,3-dihydro-1H-naphtho[1,8-de][1,3,2]diazaborinine 
• 1008097-08-2 C₂₄H₁₉BN₂ 
• 950511-11-2 4-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4'-methoxy-1,1'-biphenyl 
• 950511-24-7 4-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-2',6'-dimethyl-1,1'-biphenyl 
• 950511-23-6 4-(2,3-dihydro-1H-naphtho[1,8-de]-1,3,2-diazaborinyl)-4'-fluoro-1,1'-biphenyl 
• 446311-34-8 2-(4'-methoxy-[1,1^,-biphenyl]-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 
• 668493-36-5 (4’-(diphenylamino)-[ 1,1‘-biphenyl]-4-yl)boronic acid 
• 1072960-84-9 (4-(1H-naphtho[1,8-de][1,3,2]diazaborinin-2(3H)-yl)phenyl)methanol 
• 1207728-19-5 C₃₁H₃₅BN₂ 

Relevant articles and documents

The method for producing the phenyl boronic acid ester

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

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NiCl2(PMe3)2-catalyzed borylation of aryl chlorides

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.

Flexible synthesis, structural determination, and synthetic application of a new C1-symmetric chiral ammonium betaine

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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.