Benzenesulfonyl chloride, 2-bromo-4-fluoro-


Chemical Name: Benzenesulfonyl chloride, 2-bromo-4-fluoro-
CAS Number: 351003-45-7
Product Number: AG003B6G(AGN-PC-0KKYQO)
Synonyms:
MDL No:
Molecular Formula: C6H3BrClFO2S
Molecular Weight: 273.5072

Identification/Properties


Properties
MP:
37-39 °C
BP:
317.945 °C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Stability:
Moisture Sensitive
Refractive Index:
n20/D 1.5780(lit.)
Computed Properties
Molecular Weight:
273.5g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
271.871g/mol
Monoisotopic Mass:
271.871g/mol
Topological Polar Surface Area:
42.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
251
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information


GHS Pictogram:
Signal Word:
Danger
UN#:
2920
Hazard Statements:
H226-H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8,3
Packing Group:

NMR Spectrum


Other Analytical Data


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Chemical Structure



2-Bromo-4-fluorobenzene-1-sulfonyl chloride, also known as $name$, is a versatile chemical compound widely used in organic synthesis. This compound plays a crucial role in various chemical reactions due to its unique properties and reactivity.One of the primary applications of 2-Bromo-4-fluorobenzene-1-sulfonyl chloride is as a sulfonylating agent in organic synthesis. It is commonly used to introduce the sulfonyl group onto other organic molecules, serving as a key building block in the preparation of complex organic compounds. By acting as a sulfonylation reagent, this compound enables the selective modification of target molecules, allowing chemists to create specific structural motifs and functional groups in a controlled manner.Moreover, 2-Bromo-4-fluorobenzene-1-sulfonyl chloride can also serve as a versatile intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Its ability to undergo various chemical transformations, such as nucleophilic substitution reactions, makes it a valuable precursor for the preparation of biologically active compounds and advanced materials.In addition to its role in chemical synthesis, 2-Bromo-4-fluorobenzene-1-sulfonyl chloride is widely used in academic research and industrial applications. Its unique combination of bromo and fluoro substituents, along with the sulfonyl chloride functional group, makes it a valuable tool for exploring new synthetic methodologies and developing innovative chemical processes.Overall, 2-Bromo-4-fluorobenzene-1-sulfonyl chloride is a versatile and essential compound in the field of organic chemistry, playing a crucial role in enabling the synthesis of complex molecules with tailored properties and functions.