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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)-

Cyclopropanemethanol, 1-(4-bromophenyl)-

OCC1(CC1)c1ccc(cc1)Br Request for Quotation
Chemical Name: Cyclopropanemethanol, 1-(4-bromophenyl)-
CAS Number: 98480-31-0
Product Number: AG005UXS(AGN-PC-02OXWF)
Synonyms:
MDL No:
Molecular Formula: C10H11BrO
Molecular Weight: 227.0977

Identification/Properties

Properties
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
227.101g/mol
XLogP3:
2.5
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
225.999g/mol
Monoisotopic Mass:
225.999g/mol
Topological Polar Surface Area:
20.2A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
157
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:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Cyclopropanemethanol​, 1-​(4-​bromophenyl)​- is a versatile compound used in various chemical synthesis applications. Its unique structure containing a cyclopropane ring and a bromophenyl group offers opportunities for creating complex organic molecules with specific properties.In chemical synthesis, Cyclopropanemethanol​, 1-​(4-​bromophenyl)​- can be employed as a building block or intermediate in the preparation of biologically active compounds, pharmaceuticals, agrochemicals, and materials science. The presence of the bromophenyl group enhances the reactivity of the molecule, allowing for selective functionalization and facilitating the formation of new carbon-carbon or carbon-heteroatom bonds.This compound can participate in various synthetic transformations such as cross-coupling reactions, nucleophilic substitutions, or cycloadditions to access structurally diverse products. Its cyclopropane moiety can serve as a rigid scaffold in molecular design, influencing the stereochemistry and overall three-dimensional shape of the synthesized molecules.Overall, Cyclopropanemethanol​, 1-​(4-​bromophenyl)​- is a valuable tool in the hands of synthetic chemists for constructing intricate molecular architectures and exploring new chemical reactivity pathways in the realm of organic synthesis.