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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)-

5-bromo-3-(bromomethyl)-2-chlorothiophene

BrCc1cc(sc1Cl)Br Request for Quotation
Chemical Name: 5-bromo-3-(bromomethyl)-2-chlorothiophene
CAS Number: 1185727-35-8
Product Number: AG003MI2(AGN-PC-0BEPOS)
Synonyms:
MDL No:
Molecular Formula: C5H3Br2ClS
Molecular Weight: 290.4033

Identification/Properties

Properties
Storage:
Keep in dry area;2-8℃;
Computed Properties
Molecular Weight:
290.397g/mol
XLogP3:
4.1
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
289.799g/mol
Monoisotopic Mass:
287.801g/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

NMR Spectrum

Other Analytical Data

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Chemical Structure


5-Bromo-3-(bromomethyl)-2-chlorothiophene is a versatile compound widely utilized in chemical synthesis for its unique reactivity and functional group properties. This compound serves as a valuable building block in the synthesis of various complex organic molecules and pharmaceutical intermediates. In particular, its halogenated nature makes it a valuable precursor in the preparation of heterocyclic compounds, agrochemicals, and materials science. The presence of bromine and chlorine atoms on the thiophene ring allows for selective functionalization and cross-coupling reactions, enabling the easy introduction of diverse substituents and structural modifications. Moreover, the bromomethyl group provides a handle for further derivatization, making this compound a key intermediate in the synthesis of biologically active compounds and advanced materials. By leveraging the reactivity of 5-Bromo-3-(bromomethyl)-2-chlorothiophene, chemists can access a wide range of novel molecules and optimize synthetic routes for efficient and sustainable chemical production.