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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)-

4-Bromo-3-fluorothiophenol

Sc1ccc(c(c1)F)Br Request for Quotation
Chemical Name: 4-Bromo-3-fluorothiophenol
CAS Number: 942473-86-1
Product Number: AG00II01(AGN-PC-0WBRAL)
Synonyms:
MDL No: MFCD09475476
Molecular Formula: C6H4BrFS
Molecular Weight: 207.0634

Identification/Properties

Computed Properties
Molecular Weight:
207.06g/mol
XLogP3:
2.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
205.92g/mol
Monoisotopic Mass:
205.92g/mol
Topological Polar Surface Area:
1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
99.1
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#:
1759
Hazard Statements:
H302-H314
Precautionary Statements:
P501-P260-P270-P264-P280-P303+P361+P353-P301+P330+P331-P363-P301+P312+P330-P304+P340+P310-P305+P351+P338+P310-P405
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


4-Bromo-3-fluorobenzenethiol, also known as $name$, is a valuable compound used in chemical synthesis for its unique properties and applications. This compound serves as a versatile building block in organic chemistry, enabling the synthesis of various complex molecules and materials.In chemical synthesis, 4-Bromo-3-fluorobenzenethiol can be employed as a key reagent for introducing specific functional groups or structural motifs into target molecules. Its bromo and fluoro substituents provide opportunities for selective reactions and modifications in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals.Additionally, 4-Bromo-3-fluorobenzenethiol can function as a nucleophilic or electrophilic reactant in cross-coupling reactions, substitution reactions, and other transformations. Its distinct chemical structure allows for regioselective and stereoselective control in various synthetic pathways. By incorporating this compound into synthesis strategies, chemists can access diverse chemical space and achieve precise molecular design.Overall, 4-Bromo-3-fluorobenzenethiol plays a crucial role in advancing chemical synthesis capabilities and facilitating the creation of novel compounds with tailored properties and functionalities. Its utility and versatility make it a valuable tool for researchers and practitioners in the field of organic chemistry.