2-Bromo-4-fluorobenzenesulfonyl chloride, 97%, Thermo Scientific Chemicals
2-Bromo-4-fluorobenzenesulfonyl chloride, 97%, Thermo Scientific Chemicals
Thermo Scientific Chemicals

2-Bromo-4-fluorobenzenesulfonyl chloride, 97%, Thermo Scientific Chemicals

Have Questions?
Change viewbuttonViewtableView
Quantity:
5 g
1 g
Catalog number L19713.06
also known as L19713-06
Price (USD)/ Each
194.00
-
Add to cart
Quantity:
5 g
Request bulk or custom format
Price (USD)/ Each
194.00
Add to cart
2-Bromo-4-fluorobenzenesulfonyl chloride, 97%, Thermo Scientific Chemicals
Catalog numberL19713.06
Price (USD)/ Each
194.00
-
Add to cart
Chemical Identifiers
CAS351003-45-7
IUPAC Name2-bromo-4-fluorobenzene-1-sulfonyl chloride
Molecular FormulaC6H3BrClFO2S
InChI KeyGJPWPFVLPNTOOL-UHFFFAOYSA-N
SMILESFC1=CC(Br)=C(C=C1)S(Cl)(=O)=O
View more
SpecificationsSpecification SheetSpecification Sheet
Appearance (Color)Colorless to pale cream to pale yellow
Refractive Index1.5750-1.5800 @ 20?C
Assay (GC)≥96.0%
Melting Point (clear melt)33.0-42.0?C
FormFused solid or clear liquid as melt
View more
2-Bromo-4-fluorobenzenesulfonyl chloride is used as a pharmaceutical intermediate.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
2-Bromo-4-fluorobenzenesulfonyl chloride is used as a pharmaceutical intermediate.

Solubility
Hydrolyzes in water.

Notes
Moisture sensitive. Store away from oxidizing agents, water/ moisture, bases.
RUO – Research Use Only

General References:

  1. Ashit K. Ganguly; Sesha S. Alluri; Danielle Caroccia; Dipshikha Biswas; Chih-Hung Wang; Eunhee Kang; Yong Zhang; Andrew T. McPhail; Steven S. Carroll; Christine Burlein; Vandna Munshi; Peter Orth and Corey Strickland. Design, Synthesis, and X-ray Crystallographic Analysis of a Novel Class of HIV-1 Protease Inhibitors. J. Med. Chem. 2011, 54, (20), 7176-7183.
  2. Ashit K. Ganguly; Sesha S. Alluri; Chih-Hung Wang; Alyssa Antropow; Alex White; Danielle Caroccia; Dipshikha Biswas; Eunhee Kang; Li-Kang Zhang; Steven S. Carroll; Christine Burlein; John Fay; Peter Orthd, Corey Strickland.Structural optimization of cyclic sulfonamide based novel HIV-1 protease inhibitors to picomolar affinities guided by X-ray crystallographic analysis. Tetrahedron. 2014, 70, (18), 2894-2904.