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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, 3,4-dibromo-2,5-dichloro-

Clc1sc(c(c1Br)Br)Cl Request for Quotation
Chemical Name: Thiophene, 3,4-dibromo-2,5-dichloro-
CAS Number: 40477-45-0
Product Number: AG003IFM(AGN-PC-0LW6LF)
Synonyms:
MDL No:
Molecular Formula: C4Br2Cl2S
Molecular Weight: 310.8218

Identification/Properties

Properties
MP:
75-77°C
Storage:
Keep in dry area;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
310.812g/mol
XLogP3:
4.9
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
309.744g/mol
Monoisotopic Mass:
307.746g/mol
Topological Polar Surface Area:
28.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
101
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


3,4-Dibromo-2,5-dichlorothiophene, with its unique molecular structure, finds extensive application in chemical synthesis as a versatile building block and intermediate. This compound is utilized in the synthesis of various organic molecules and materials due to its reactivity and selectivity in forming complex structures. In particular, 3,4-Dibromo-2,5-dichlorothiophene is commonly employed in the preparation of pharmaceuticals, agrochemicals, and advanced materials such as polymers and liquid crystals. Its distinct halogen functionalities enable precise control over chemical reactions and regioselectivity, making it a valuable tool for synthetic chemists seeking to introduce specific functionalities into target compounds. By serving as a key component in diverse synthetic pathways, 3,4-Dibromo-2,5-dichlorothiophene plays a crucial role in enabling the creation of new molecules with tailored properties and applications.