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264431

Sigma-Aldrich

2,6-Difluorobenzyl bromide

97%

Synonym(s):

α-Bromo-2,6-difluorotoluene

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About This Item

Linear Formula:
F2C6H3CH2Br
CAS Number:
Molecular Weight:
207.02
Beilstein:
2083943
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

form

solid

mp

52-55 °C (lit.)

functional group

bromo
fluoro

SMILES string

Fc1cccc(F)c1CBr

InChI

1S/C7H5BrF2/c8-4-5-6(9)2-1-3-7(5)10/h1-3H,4H2

InChI key

LSXJPJGBWSZHTM-UHFFFAOYSA-N

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Application

2,6-Difluorobenzyl bromide has been used:
  • as reagent in alkylation of the quinazoline-2-thioxo-4-one
  • in the synthesis of 1,3,5-triazine-2,4,6-triones
  • in the preparation of new classes of inhibitors of bovine viral diarrhea virus (as a surrogate virus for hepatitis C virus)

Pictograms

Corrosion

Signal Word

Danger

Hazard Statements

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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A convenient one-pot synthetic route was developed for the preparation of asymmetric 1,3-dialkyl-1,3,5-triazine-2,4,6-triones from readily available alkyl- or aryl-isocyanates, primary amines and N-chlorocarbonyl isocyanate in excellent yields. Subsequent alkylation with N-protected amino alcohols afforded the desired 1,3,5-triazine-2,4,6-triones in good yields.
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