1002727-88-9

Basic information

• Product Name: 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman, 97%
• Synonyms: 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman, 97%;3,4-Dihydro-2H-chromene-6-boronic acid, pinacol ester, 3,4-Dihydro-6-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2H-chromene;Chroman-6-boronic acid, pinacol ester;2-(ChroMan-6-yl)-4,4,5,5-tetraMethyl-1,3,2-dioxaborolane
• CAS NO: 1002727-88-9
• Molecular Formula: C₁₅H₂₁BO₃
• Molecular Weight: 260
• Product Categories: Organic boronic acid
• Mol File: 1002727-88-9.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 373.5±31.0 °C(Predicted)
• Appearance: /
• Density: 1.08±0.1 g/cm3(Predicted)
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• CAS DataBase Reference: 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman, 97%(CAS DataBase Reference)
• NIST Chemistry Reference: 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman, 97%(1002727-88-9)
• EPA Substance Registry System: 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman, 97%(1002727-88-9)

Safety Data

• Hazardous Substances Data: 1002727-88-9(Hazardous Substances Data)

Usage

General Description

6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman, 97% is a chemical compound with a high purity level of 97%. It consists of a chroman molecule attached to a boron-containing group, specifically a 4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl substituent. 6-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)chroman, 97% is often used as a reactant in organic synthesis, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is also utilized in the production of pharmaceuticals, agrochemicals, and materials science. Due to its high purity, this chemical is suitable for use in research and industrial applications where precise and reliable results are required.

Upstream product

• 3875-78-3 6-bromo-chroman 
• 73183-34-3 bis(pinacol)diborane 
• 493-08-3 chromane 
• 67856-45-5 6-iodo-chroman 
• 491-37-2 2,3-dihydro-4H-1-benzopyran-4-one 

Downstream Products

• 1155288-15-5 C₃₂H₃₃NO₅ 
• 1403382-26-2 methyl 2-[3-(benzyloxy)-2-(3,4-dihydro-2H-1-benzopyran-6-yl)-6-(trifluoromethyl)phenyl]-2-oxoacetate 
• 1403382-27-3 methyl 2-[3-(benzyloxy)-2-(3,4-dihydro-2H-1-benzopyran-6-yl)-6-(trifluoromethyl)phenyl]-2-hydroxyacetate 
• 1596341-39-7 methyl 2-[2-(3,4-dihydro-2H-1-benzopyran-6-yl)-3-(3-phenyl-1H-pyrazol-1-yl)-6-(trifluoromethyl)phenyl]-2-oxoacetate 
• 1596341-40-0 methyl 2-[2-(3,4-dihydro-2H-1-benzopyran-6-yl)-3-(3-phenyl-1H-pyrazol-1-yl)-6-(trifluoromethyl)phenyl]-2-hydroxyacetate 
• 1155288-14-4 C₃₁H₃₁NO₅ 
• 1403382-23-9 methyl 2-[2-(3,4-dihydro-2H-1-benzopyran-6-yl)-3-fluoro-6-(trifluoromethyl)phenyl]-2-oxoacetate 
• 1596341-32-0 2-[2-(3,4-dihydro-2H-1-benzopyran-6-yl)-3-fluoro-6-(trifluoromethyl)phenyl]-2-oxoacetic acid 
• 1596367-40-6 methyl 2-[3-benzyloxy-2-(3,4-dihydro-2H-1-benzopyran-6-yl)-6-methylphenyl]-2-hydroxyacetate 
• 1596341-13-7 2-(tert-butoxy)-2-[2-(3,4-dihydro-2H-1-benzopyran-6-yl)-3-phenyl-6-(trifluoromethyl)phenyl]acetic acid 

Relevant articles and documents

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The present invention relates to a novel organic electroluminescent compound which is represented by the following [chemical formula 1] or [chemical formula 2]. The electroluminescent compound according to the present invention has high glass transition temperature, thereby having enhanced thermal stability; and can form an organic electroluminescent device having low driving voltage, high luminance, high color purity, and long-life when applying the same to the electroluminescent device.

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Compounds of formula I : wherein c, R2, R3, R4, R5, R6, R7 and R8 are defined herein, are useful as inhibitors of HIV replication.

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Compounds of formula (I): wherein c, X, Y, R2, R4 and R5 are defined herein, are useful as inhibitors of HIV replication.