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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, 2,4-dibromo-

Brc1scc(c1)Br Request for Quotation
Chemical Name: Thiophene, 2,4-dibromo-
CAS Number: 3140-92-9
Product Number: AG0032YV(AGN-PC-0KK0C7)
Synonyms:
MDL No:
Molecular Formula: C4H2Br2S
Molecular Weight: 241.9317

Identification/Properties

Properties
MP:
-26.3°C
BP:
213.4°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Refractive Index:
1.631-1.633
Computed Properties
Molecular Weight:
241.928g/mol
XLogP3:
3.3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
241.822g/mol
Monoisotopic Mass:
239.824g/mol
Topological Polar Surface Area:
28.2A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
66.7
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#:
2810
Hazard Statements:
H301-H315-H318-H335
Precautionary Statements:
P261-P280-P301+P310-P305+P351+P338
Class:
6.1
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4-Dibromothiophene is a highly versatile compound widely used in chemical synthesis processes. This compound plays a crucial role in the production of various pharmaceuticals, agrochemicals, and materials due to its unique properties and reactivity.In chemical synthesis, 2,4-Dibromothiophene serves as a key building block for the construction of complex organic molecules. Its bromine functional groups allow for selective and controlled reactions, making it valuable in the formation of new carbon-carbon and carbon-heteroatom bonds.One important application of 2,4-Dibromothiophene is its use in the development of novel pharmaceuticals. By incorporating this compound into drug molecules, chemists can fine-tune the pharmacological properties and optimize the biological activity of the final product.Additionally, 2,4-Dibromothiophene is utilized in the synthesis of agrochemicals, such as pesticides and herbicides. Its sulfur-containing ring confers unique chemical properties that are beneficial for enhancing the effectiveness and selectivity of agricultural products.Moreover, 2,4-Dibromothiophene finds applications in materials science, where it can be incorporated into polymers, dyes, and organic electronic materials. Its presence can impart desirable properties such as improved solubility, conductivity, or optical characteristics to the final material.Overall, the versatility and reactivity of 2,4-Dibromothiophene make it a valuable tool for chemists in designing and synthesizing a wide range of compounds with diverse applications in pharmaceuticals, agrochemicals, and materials science.