Skip to Content
Merck
CN

542733

4-Fluorobenzenesulfonamide

98%

Sign In to View Organizational & Contract Pricing.

Select a Size

About This Item

Linear Formula:
FC6H4SO2NH2
CAS Number:
402-46-0
Molecular Weight:
175.18
NACRES:
NA.22
PubChem Substance ID:
24878629
UNSPSC Code:
12352100
EC Number:
206-946-2
MDL number:
MFCD00025384

Key Documents

View All Documentation
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

4-Fluorobenzenesulfonamide, 98%

InChI key

LFLSATHZMYYIAQ-UHFFFAOYSA-N

InChI

1S/C6H6FNO2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H,(H2,8,9,10)

SMILES string

NS(=O)(=O)c1ccc(F)cc1

assay

98%

mp

124-127 °C (lit.)

Application

4-Fluorobenzenesulfonamide may be used to synthesize 4-fluorophenylsulfonyldithiocarbimate potassium dihydrate and amino-substituted sulfanilamide derivatives.

General description

4-Fluorobenzenesulfonamide is a para-halogen benzenesulfonamide. Ab initio Hartree-Fock (HF) and density functional theory (DFT) have been used to investigate the structural features of 4-fluorobenzenesulfonamide.

signalword

Warning

pictograms

Exclamation mark
GHS07

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

Regulatory Information

新产品
This item has

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number
MKCR3446
MKCS5851
MKBK3845V
MKBH9881V
11017LH

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Search for a COA

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Guillaume Compain et al.
Bioorganic & medicinal chemistry, 21(6), 1555-1563 (2012-06-19)
A series of new, halogen containing N-substituted 4-aminobenzenesulfonamides were synthesized by using superacid HF/SbF5 chemistry and investigated as inhibitors of several human carbonic anhydrase (hCA, EC 4.2.1.1) isoforms, that is, the cytosolic hCA I and II and, the tumor-associated transmembrane
L B Dugad et al.
Biochemistry, 27(12), 4310-4316 (1988-06-14)
Binding of 4-fluorobenzenesulfonamide to human carbonic anhydrases I and II has been studied by proton, fluorine, and nitrogen-15 nuclear magnetic resonance spectroscopy. All three types of experiments provide evidence that the stoichiometry of the interaction of this inhibitor with both
Theoretical investigation on the molecular structure, Infrared, Raman and NMR spectra of para-halogen benzenesulfonamides, 4-XC6H4SO2NH2 (X= Cl, Br or F).
Karabacak M, et al.
Journal of Molecular Structure, 919(1), 26-33 (2009)
Bis (4-fluorophenylsulfonyldithiocarbimato) zincate (ii) salts: new antifungals for the control of botrytis blight.
Oliveira AA, et al.
Quimica nova, 38(6), 757-761 (2015)

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

Contact Technical Service