Manufacturer supply high quality 4-tert-Butylphenylboronic acid 123324-71-0 with GMP standards
- Molecular Formula:C10H15BO2
- Molecular Weight:178.039
- Appearance/Colour:white to off-white crystalline powder
- Vapor Pressure:0mmHg at 25°C
- Melting Point:193-199 ºC
- Refractive Index:1.59
- Boiling Point:296.7 ºC at 760 mmHg
- PKA:8.79±0.10(Predicted)
- Flash Point:133.2 ºC
- PSA：40.46000
- Density:1.02 g/cm2
- LogP:0.66390
4-tert-Butylphenylboronic acid(Cas 123324-71-0) Usage
4-tert-Butylphenylboronic acid is a biochemical reagent used in various scientific research fields, including organic synthesis, pharmaceutical development, and material science.
InChI:InChI=1/C7H7BO4/c9-8(10)5-1-2-6-7(3-5)12-4-11-6/h1-3,9-10H,4H2
123324-71-0 Relevant articles
Synthesis of t-butylated diphenylanthracene derivatives as blue host materials for OLED applications
Balaganesan, Banumathy,Shen, Wen-Jian,Chen, Chin H.
, p. 5747 - 5750 (2003)
This paper describes the cost-effective ...
New C2v- and chiral C2-symmetric olefin polymerization catalysts based on nickel(II) and palladium(II) diimine complexes bearing 2,6-diphenyl aniline moieties: Synthesis, structural characterization, and first insight into polymerization properties
Schmid, Markus,Eberhardt, Robert,Klinga, Martti,Leskel?, Markku,Rieger, Bernhard
, p. 2321 - 2330 (2001)
Four new 1,4-diaza-2,3-dimethylbutadiene...
Spectroscopic and computational investigations of the thermodynamics of boronate ester and diazaborole self-assembly
Goldberg, Alexander R.,Northrop, Brian H.
, p. 969 - 980 (2016)
The solution phase self-assembly of boro...
Transition-Metal-Free Borylation of Aryl Bromide Using a Simple Diboron Source
Han, Min Su,Lim, Taeho,Ryoo, Jeong Yup
, p. 10966 - 10972 (2020/09/23)
In this study, we developed a simple tra...
Iron catalysis and water: A synergy for refunctionalization of boron
Wood, John L.,Marciasini, Ludovic D.,Vaultier, Michel,Pucheault, Mathieu
supporting information, p. 551 - 555 (2014/03/21)
A new catalytic system has been optimize...
Vaulted biaryls in catalysis: A structure-activity relationship guided tour of the immanent domain of the VANOL ligand
Guan, Yong,Ding, Zhensheng,Wulff, William D.
supporting information, p. 15565 - 15571 (2013/11/19)
The active site in the BOROX catalyst is...
123324-71-0 Process route
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- 98-29-3
4-tert-Butylcatechol
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- 123324-71-0
p-tert-butylphenylboronic acid
Conditions
| Conditions |
Yield |
|
In chloroform-d1; at 25 ℃; Equilibrium constant; Sealed tube;
|
|
-
-
potassium (4-tert-butyl)phenyltrifluoroborate
-
- 123324-71-0
p-tert-butylphenylboronic acid
Conditions
| Conditions |
Yield |
|
With 1H-imidazole; iron(III) chloride; at 20 ℃; for 0.25h; Inert atmosphere;
|
85% |
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-
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-
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