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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)-

(1-(4-broMophenyl)cyclobutyl)Methanol

OCC1(CCC1)c1ccc(cc1)Br Request for Quotation
Chemical Name: (1-(4-broMophenyl)cyclobutyl)Methanol
CAS Number: 1227159-85-4
Product Number: AG000J1G(AGN-PC-0WAK5P)
Synonyms:
MDL No:
Molecular Formula: C11H13BrO
Molecular Weight: 241.1243

Identification/Properties

Computed Properties
Molecular Weight:
241.128g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
240.015g/mol
Monoisotopic Mass:
240.015g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
169
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


The (1-(4-Bromophenyl)cyclobutyl)methanol compound is a versatile building block in chemical synthesis. It serves as a valuable intermediate for the preparation of various pharmaceuticals, agrochemicals, and specialty chemicals due to its unique structural properties. This molecule can be utilized in the synthesis of complex organic compounds through functional group interconversions, structural modifications, and cascade reactions. Additionally, the (1-(4-Bromophenyl)cyclobutyl)methanol can be employed as a chiral building block for the construction of enantioenriched molecules, making it a valuable tool in asymmetric synthesis strategies. Its reactivity and compatibility with a wide range of synthetic methodologies make it a valuable asset in the toolbox of organic chemists aiming to access diverse chemical space for the discovery of new materials and biologically active compounds.