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578401

Sigma-Aldrich

3-Cyanophenylboronic acid pinacol ester

97%

Synonym(s):

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

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About This Item

Empirical Formula (Hill Notation):
C13H16BNO2
CAS Number:
Molecular Weight:
229.08
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

mp

78-82 °C (lit.)

SMILES string

CC1(C)OB(OC1(C)C)c2cccc(c2)C#N

InChI

1S/C13H16BNO2/c1-12(2)13(3,4)17-14(16-12)11-7-5-6-10(8-11)9-15/h5-8H,1-4H3

InChI key

FIGQEPXOSAFKTA-UHFFFAOYSA-N

Application

3-Cyanophenylboronic acid pinacol ester can be used as a reactant to synthesize:
  • 3-Cyano aryl/ heteroaryl derivatives by forming a C−C bond via palladium-catalyzed Suzuki-Miyaura reaction.
  • 3-(Phenylamino)benzonitrile by copper-catalyzed Chan-Evans-Lam amination reaction.
  • 3-(Trifluoromethyl)benzonitrile using potassium (trifluoromethyl)trimethoxyborate.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

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

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Chan-Evans-Lam amination of boronic acid pinacol (BPin) esters: overcoming the aryl amine problem
Vantourout JC, et al.
The Journal of Organic Chemistry, 81(9), 3942-3950 (2016)
Oxidative Trifluoromethylation of Arylboronates with Shelf-Stable Potassium (Trifluoromethyl) trimethoxyborate
Khan BA, et al.
Chemistry?A European Journal , 18(6), 1577-1581 (2012)
Speciation control during Suzuki-Miyaura cross-coupling of haloaryl and haloalkenyl MIDA boronic esters
Fyfe JWB, et al.
Chemistry?A European Journal , 21(24), 8951-8964 (2015)

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