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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)-

Furan, 3-(bromomethyl)tetrahydro-

BrCC1COCC1 Request for Quotation
Chemical Name: Furan, 3-(bromomethyl)tetrahydro-
CAS Number: 165253-29-2
Product Number: AG001W0S(AGN-PC-000JG1)
Synonyms:
MDL No:
Molecular Formula: C5H9BrO
Molecular Weight: 165.0284

Identification/Properties

Computed Properties
Molecular Weight:
165.03g/mol
XLogP3:
1.2
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
1
Exact Mass:
163.984g/mol
Monoisotopic Mass:
163.984g/mol
Topological Polar Surface Area:
9.2A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
56
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
1
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:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Bromomethyl)tetrahydrofuran is a versatile chemical compound widely used in chemical synthesis as a valuable building block. Its unique structure allows for a range of applications in organic chemistry, particularly in the formation of various functionalized compounds and heterocyclic derivatives. One key application of 3-(Bromomethyl)tetrahydrofuran is in the synthesis of pharmaceuticals and agrochemicals. Its bromomethyl group provides a reactive site for further functionalization, allowing chemists to introduce specific moieties or structural motifs necessary for biological activity. This compound serves as an essential intermediate in the production of complex molecules with therapeutic or pesticidal properties. Furthermore, 3-(Bromomethyl)tetrahydrofuran plays a crucial role in the preparation of advanced materials such as polymers and fine chemicals. Through strategic manipulations of its chemical reactivity, researchers can access a diverse array of molecular architectures that are vital for the development of innovative materials with tailored properties. The presence of the bromine atom in this compound enables efficient cross-coupling reactions, facilitating the construction of intricate molecular frameworks.In summary, 3-(Bromomethyl)tetrahydrofuran is a valuable tool in the toolbox of synthetic chemists, enabling the construction of complex molecules for various applications in the fields of pharmaceuticals, agrochemicals, materials science, and beyond.