522554
2-Hydroxyphenylboronic acid pinacol ester
98%
Synonym(s):
2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol
About This Item
Recommended Products
Assay
98%
refractive index
n20/D 1.506 (lit.)
bp
282 °C (lit.)
density
1.05 g/mL at 25 °C (lit.)
SMILES string
CC1(C)OB(OC1(C)C)c2ccccc2O
InChI
1S/C12H17BO3/c1-11(2)12(3,4)16-13(15-11)9-7-5-6-8-10(9)14/h5-8,14H,1-4H3
InChI key
VLROJECCXBBKPZ-UHFFFAOYSA-N
Application
- Synthesis of indolo-fused heterocyclic inhibitors of polymerase enzyme of hepatitis C
- Studies of pi-interactions, electronic structure and transient UV absorption of subphthalocyanine-borate-bridged ferrocene-fullerene conjugates
- Synthesis of subphthalocyanine and fused-ring nicotine derivatives
- Suzuki-Miyaura coupling-triflation sequence, reduction and salt formation for synthesis of hydroxylated oligoarene phosphines
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Regulatory Listings
Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.
FSL
Group 4: Flammable liquids
Type 3 petroleums
Hazardous rank III
Water insoluble liquid
JAN Code
522554-BULK:
522554-1G:
522554-5G:
522554-VAR:
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Articles
The synthesis of biaryl compounds via the Suzuki coupling reaction has become more commonplace now that many arylboronic acids are readily available. We are pleased to offer arylboronic acid pinacol esters4 as part of a growing line of products used in the Suzuki coupling reaction.
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