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Sigma-Aldrich

2-Bromo-5-fluorobenzonitrile

95%

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About This Item

Linear Formula:
BrC6H3(F)CN
CAS Number:
Molecular Weight:
200.01
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

95%

mp

92-95 °C (lit.)

SMILES string

Fc1ccc(Br)c(c1)C#N

InChI

1S/C7H3BrFN/c8-7-2-1-6(9)3-5(7)4-10/h1-3H

InChI key

MDHNVHCZDCSTMS-UHFFFAOYSA-N

General description

2-Bromo-5-fluorobenzonitrile can be prepared from 3-fluorobenzonitrile vial bromination using 1,3-dibromo-5,5-dimethylhydantoin (DBDMH).. It undergoes palladium-catalyzed Suzuki coupling with boronic acid derivative to form corresponding biaryl.

Application

2-Bromo-5-fluorobenzonitrile may be used in the preparation of 5-chloro-4,2?-difluorobiphenyl-2-carbonitrile.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

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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Large-scale applications of transition metal-catalyzed couplings for the synthesis of pharmaceuticals.
Magano J and Dunetz JR.
Chemical Reviews, 111(3), 2177-2250 (2011)
The Expedient Synthesis of 4, 2'-Difluoro-5'-(7-trifluoromethyl-imidazo [1,2-a] pyrimidin-3-yl) biphenyl-2-carbonitrile, a GABA ?2/3 Agonist.
Cameron M, et al.
Organic Process Research & Development, 10(3), 398-402 (2006)
Facile synthesis of 2-bromo-3-fluorobenzonitrile: An application and study of the halodeboronation of aryl boronic acids.
Szumigala RH, et al.
The Journal of Organic Chemistry, 69(2), 566-569 (2004)

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