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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)-

2,2'-Bithiophene, 4,4'-dibromo-

Brc1csc(c1)c1scc(c1)Br Request for Quotation
Chemical Name: 2,2'-Bithiophene, 4,4'-dibromo-
CAS Number: 51285-60-0
Product Number: AG00DC0K(AGN-PC-0JVD1S)
Synonyms:
MDL No:
Molecular Formula: C8H4Br2S2
Molecular Weight: 324.0554

Identification/Properties

Properties
MP:
132.0 to 136.0℃
Form:
Solid
Computed Properties
Molecular Weight:
324.048g/mol
XLogP3:
4.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
323.81g/mol
Monoisotopic Mass:
321.812g/mol
Topological Polar Surface Area:
56.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
147
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


In chemical synthesis, 4,4'-Dibromo-2,2'-bithiophene serves as a versatile building block for the construction of various organic compounds. Known for its unique structure, this compound is widely utilized in the preparation of advanced materials such as conducting polymers and organic semiconductors. Its bromine substituents enable selective functionalization reactions, allowing for the precise modification of its chemical properties. Through cross-coupling reactions and other synthetic methodologies, 4,4'-Dibromo-2,2'-bithiophene can be incorporated into complex molecular architectures, offering researchers a valuable tool for designing and synthesizing novel organic molecules with tailored electronic and optical properties.