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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)-

Thieno[3,2-b]thiophene, 3-bromo-

Brc1csc2c1scc2 Request for Quotation
Chemical Name: Thieno[3,2-b]thiophene, 3-bromo-
CAS Number: 25121-83-9
Product Number: AG002QJY(AGN-PC-0018TM)
Synonyms:
MDL No:
Molecular Formula: C6H3BrS2
Molecular Weight: 219.1220

Identification/Properties

Properties
BP:
287.952°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Refractive Index:
1.6850-1.6890
Computed Properties
Molecular Weight:
219.114g/mol
XLogP3:
3.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
217.886g/mol
Monoisotopic Mass:
217.886g/mol
Topological Polar Surface Area:
56.5A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
118
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-Bromothieno[3,2-b]thiophene is a versatile compound widely used in organic synthesis as a building block in the creation of various chemical compounds. Its unique structure and reactivity make it a valuable tool in the preparation of organic molecules with diverse functionalities. One key application of 3-Bromothieno[3,2-b]thiophene is its role as a key intermediate in the synthesis of organic semiconductors. By incorporating this compound into the molecular structure of semiconducting materials, researchers can tailor the electronic properties of the final product for use in electronic devices such as organic light-emitting diodes (OLEDs), field-effect transistors (FETs), and solar cells.Additionally, 3-Bromothieno[3,2-b]thiophene is utilized in the synthesis of pharmaceutical compounds, agrochemicals, and materials science. Its presence in the molecular structure imparts specific properties and functions to the final products, making it an indispensable building block in the field of chemical synthesis.Overall, 3-Bromothieno[3,2-b]thiophene plays a crucial role in the development of advanced materials and functional organic molecules due to its unique structural features and reactivity in chemical reactions.