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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Sulfur, [4-(chlorocarbonyl)phenyl]pentafluoro-, (OC-6-21)-

ClC(=O)c1ccc(cc1)S(F)(F)(F)(F)F Request for Quotation
Chemical Name: Sulfur, [4-(chlorocarbonyl)phenyl]pentafluoro-, (OC-6-21)-
CAS Number: 197384-98-8
Product Number: AG002AS6(AGN-PC-0QOZ8U)
Synonyms:
MDL No:
Molecular Formula: C7H4ClF5OS
Molecular Weight: 266.6161

Identification/Properties

Computed Properties
Molecular Weight:
266.61g/mol
XLogP3:
5.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
1
Exact Mass:
265.959g/mol
Monoisotopic Mass:
265.959g/mol
Topological Polar Surface Area:
18.1A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
278
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#:
1760
Hazard Statements:
H314-H318
Precautionary Statements:
P260-P264-P280-P301+P330+P331-P303+P361+P353-P304+P340-P305+P351+P338-P310-P321-P363-P405-P501
Class:
8
Packing Group:
Ⅱ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-(Pentafluorosulfanyl)benzoylchloride, a versatile chemical compound, plays a crucial role in modern chemical synthesis processes. As a key reagent in organic chemistry, it is utilized for the functionalization of various organic molecules by introducing the highly electronegative pentafluorosulfanyl group.The electrophilic nature of the benzoylchloride moiety within the compound allows for efficient acylation reactions with nucleophiles, enabling the synthesis of a wide range of complex organic compounds. Additionally, the presence of the pentafluorosulfanyl group enhances the stability and reactivity of the resulting products, making it an invaluable tool for the creation of novel chemical structures.Furthermore, 4-(Pentafluorosulfanyl)benzoylchloride exhibits unique properties that can lead to the development of new materials with enhanced properties, such as improved thermal stability and resistance to chemical degradation. Its application extends to various fields, including pharmaceuticals, agrochemicals, and materials science, demonstrating its significance in advancing chemical synthesis capabilities.