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513490

Sigma-Aldrich

4-Carboxylphenylboronic acid pinacol ester

97%

Synonym(s):

4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid

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About This Item

Empirical Formula (Hill Notation):
C13H17BO4
CAS Number:
180516-87-4
Molecular Weight:
248.08
MDL number:
MFCD01863710
UNSPSC Code:
12352103
PubChem Substance ID:
24873696
NACRES:
NA.22

Quality Level

100

Assay

97%

mp

228-231 °C (lit.)

SMILES string

CC1(C)OB(OC1(C)C)c2ccc(cc2)C(O)=O

InChI

1S/C13H17BO4/c1-12(2)13(3,4)18-14(17-12)10-7-5-9(6-8-10)11(15)16/h5-8H,1-4H3,(H,15,16)

InChI key

IYDKBQIEOBXLTP-UHFFFAOYSA-N

Related Categories

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
WXBC7455V
SHBB2010V
11696LK
82797KJ
09207EH

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Articles

Arylboronic Acid-Pinacol Esters

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.

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

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