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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)-

Thiophene, 2-bromo-5-phenyl-

Brc1ccc(s1)c1ccccc1 Request for Quotation
Chemical Name: Thiophene, 2-bromo-5-phenyl-
CAS Number: 29488-24-2
Product Number: AG002YK5(AGN-PC-0KKXFY)
Synonyms:
MDL No:
Molecular Formula: C10H7BrS
Molecular Weight: 239.1316

Identification/Properties

Properties
MP:
83 °C
BP:
289.2°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
239.13g/mol
XLogP3:
4.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
237.945g/mol
Monoisotopic Mass:
237.945g/mol
Topological Polar Surface Area:
28.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
143
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:
Warning
UN#:
-
Hazard Statements:
H317-H319
Precautionary Statements:
P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Bromo-5-phenylthiophene is a versatile chemical compound widely utilized in organic synthesis and medicinal chemistry. This unique building block is valued for its ability to introduce the phenylthiophene moiety into various molecular structures, conferring specific properties and functionalities.In chemical synthesis, 2-Bromo-5-phenylthiophene serves as a key intermediate in the preparation of biologically active compounds and functional materials. Its bromo substituent allows for selective functionalization through various cross-coupling reactions such as Suzuki, Heck, and Sonogashira couplings. This enables the efficient construction of complex molecular architectures with tailored properties.Moreover, the presence of the phenylthiophene scaffold imparts desirable electronic properties to the synthesized molecules, making them potentially useful in organic electronic devices, pharmaceuticals, and agrochemicals. The incorporation of 2-Bromo-5-phenylthiophene in chemical synthesis thus offers a strategic approach to molecular design, enabling the development of new materials and compounds with diverse applications.