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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-Pentanone, 1-(4-bromophenyl)-

CCCCC(=O)c1ccc(cc1)Br Request for Quotation
Chemical Name: 1-Pentanone, 1-(4-bromophenyl)-
CAS Number: 7295-44-5
Product Number: AG003KLG(AGN-PC-0JLTFN)
Synonyms:
MDL No:
Molecular Formula: C11H13BrO
Molecular Weight: 241.1243

Identification/Properties

Properties
MP:
34-36 °C
BP:
291.3°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Refractive Index:
1.5290 (estimate)
Computed Properties
Molecular Weight:
241.128g/mol
XLogP3:
3.7
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
4
Exact Mass:
240.015g/mol
Monoisotopic Mass:
240.015g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
160
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
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


4’-Bromovalerophenone, also known as 1-(4-bromophenyl)-1-pentanone, is a versatile chemical compound commonly utilized in organic synthesis. Its application in chemical synthesis is vast and plays a crucial role in various reactions and processes.One of the primary uses of 4’-Bromovalerophenone is as a key intermediate in the synthesis of pharmaceutical compounds. Its unique chemical structure makes it an essential building block for creating a wide range of biologically active molecules. By incorporating 4’-Bromovalerophenone into the synthesis pathway, chemists can introduce specific functional groups and modify the properties of the final target compound.Furthermore, this compound is often employed in the synthesis of fragrances and flavoring agents. Its aromatic nature and reactivity allow for the creation of complex odor molecules that are used in perfumes, cosmetics, and food products. By incorporating 4’-Bromovalerophenone into the chemical reaction, chemists can tailor the scent profile and enhance the overall fragrance composition.Additionally, 4’-Bromovalerophenone serves as a valuable precursor in the preparation of advanced materials. Its structural versatility enables the formation of polymers, coatings, and specialty chemicals with tailored properties. By utilizing this compound in the synthesis process, chemists can engineer materials with specific physical, chemical, and mechanical characteristics to meet diverse industrial demands.In summary, 4’-Bromovalerophenone plays a vital role in chemical synthesis, particularly in the creation of pharmaceuticals, fragrances, flavoring agents, and advanced materials. Its versatility and reactivity make it a valuable tool for chemists seeking to design and develop new compounds with unique properties and applications.