162356-89-0

Basic information

• Product Name: [4-[[[1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]phenylboronic Acid
• Synonyms: [4-[[[1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]phenylboronic Acid;4-TBSMS-hydroxymethylphenylboronic acid;[4-[[[tert-Butyl)dimethylsilyl]oxy]methyl]phenylboronic acid;4-TBDMSO-methylphenylboronic acid;Boronic acid, B-[4-[[[(1,1-diMethylethyl)diMethylsilyl]oxy]Methyl]phenyl]-
• CAS NO: 162356-89-0
• Molecular Formula: C₁₃H₂₃BO₃Si
• Molecular Weight: 266.219
• Mol File: 162356-89-0.mol

Chemical Properties

• Melting Point: 153-155°C
• Boiling Point: 356.1±44.0 °C(Predicted)
• Appearance: /
• Density: 1.00±0.1 g/cm3(Predicted)
• Refractive Index: 1.509
• Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
• PKA: 8.53±0.16(Predicted)
• CAS DataBase Reference: [4-[[[1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]phenylboronic Acid(CAS DataBase Reference)
• NIST Chemistry Reference: [4-[[[1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]phenylboronic Acid(162356-89-0)
• EPA Substance Registry System: [4-[[[1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]phenylboronic Acid(162356-89-0)

Safety Data

• Hazardous Substances Data: 162356-89-0(Hazardous Substances Data)

Usage

Uses

Used in Organic Synthesis:
[4-[[[1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]phenylboronic Acid is used as a reagent for the formation of carbon-carbon bonds through Suzuki coupling reactions, a widely employed method in the synthesis of complex organic molecules.
Used in the Synthesis of Complex Organic Molecules:
In the Pharmaceutical Industry, [4-[[[1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]phenylboronic Acid is used as a building block for the creation of complex organic molecules, taking advantage of its silyl-protected alcohol group and boronic acid functionality.
Used in a Wide Range of Reactions:
[4-[[[1,1-Dimethylethyl)dimethylsilyl]oxy]methyl]phenylboronic Acid is utilized in various chemical reactions due to its boronic acid functionality, making it a valuable compound in the field of organic chemistry.

InChI:InChI=1/C13H23BO3Si/c1-13(2,3)18(4,5)11-6-7-12(14(16)17)10(8-11)9-15/h6-8,15-17H,9H2,1-5H3

Upstream product

• 1072960-69-0 (C(CH₃)3Si(CH₃)2OCH₂C₆H₄)BN(CH₃)(CH₂CO₂)2 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 873-75-6 4-bromobenzenemethanol 
• 87736-74-1 4-(tert-butyldimethylsiloxymethyl)bromobenzene 

Downstream Products

• 1204190-96-4 C₈-(4-(TBS-O-methyl)phenyl)-2'-deoxyguanosine 
• 1613027-65-8 2-(4-(((tert-butyldimethylsilyl)oxy)methyl)phenyl)pyridine 
• 1613027-79-4 tert-butyl [5-(tert-butyldimethylsilyloxymethyl)-2-(pyridin-2-yl)phenyl]carbamate 
• 648424-24-2 [1,1-dimethyl-2-oxo-2-[[(3R)-2,3,4,5-tetrahydro-1-[[2'-[[[(methylamino)carbonyl]amino]methyl][1,1'-biphenyl]-4-yl]methyl]-2-oxo-1H-1-benzazepin-3-yl]amino]ethyl]carbamic acid (1,1-dimethylethyl) ester 
• 198205-99-1 2'-(aminomethyl)[1,1'-biphenyl]-4-methanol 
• 637004-43-4 ClCOOCH₂C₆H₄BO₂C₄H₈ 
• 637004-42-3 2-(4-hydroxymethyl-phenyl)-4,5-dimethyl-[1,3,2]dioxaborolane 
• 477338-82-2 2-[4-(tert-butyl-dimethyl-silanyloxymethyl)-phenyl]-4,5-dimethyl-[1,3,2]dioxaborolane 

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