1. Home
  2. Furan, 2,5-dibromo-

Contact Angene

Tel: +852 8191 6999

Email: sales@angenechemical.com

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)-

Furan, 2,5-dibromo-

Brc1ccc(o1)Br Request for Quotation
Chemical Name: Furan, 2,5-dibromo-
CAS Number: 32460-00-7
Product Number: AG003302(AGN-PC-0NC49K)
Synonyms:
MDL No:
Molecular Formula: C4H2Br2O
Molecular Weight: 225.8661

Identification/Properties

Properties
MP:
10 °C
BP:
165.3°C at 760 mmHg
Storage:
Inert atmosphere;-10 ℃;
Form:
Liquid
Refractive Index:
1.5510-1.5550
Computed Properties
Molecular Weight:
225.867g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
225.845g/mol
Monoisotopic Mass:
223.847g/mol
Topological Polar Surface Area:
13.1A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
58.7
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#:
1993
Hazard Statements:
H226
Precautionary Statements:
P501-P240-P210-P233-P243-P241-P242-P280-P370+P378-P303+P361+P353-P403+P235
Class:
3
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


2,5-Dibromofuran is a key building block in chemical synthesis due to its unique structure and reactivity. This compound is commonly utilized as a versatile intermediate in the production of various pharmaceuticals, agrochemicals, and advanced materials. Its bromine substituents make it a valuable precursor for introducing functional groups or modifying existing chemical structures, allowing for the creation of new compounds with tailored properties. In organic synthesis, 2,5-Dibromofuran serves as a potent electrophile in cross-coupling reactions, such as Suzuki-Miyaura and Heck couplings, enabling the formation of carbon-carbon bonds and the incorporation of furan motifs into complex molecules. Its role extends to the synthesis of heterocyclic compounds, natural products, and fine chemicals, making it a versatile and indispensable reagent in modern chemical research and development.