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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)-

Cyclopentanone, 2-(phenylmethyl)-

O=C1CCCC1Cc1ccccc1 Request for Quotation
Chemical Name: Cyclopentanone, 2-(phenylmethyl)-
CAS Number: 2867-63-2
Product Number: AG002W1D(AGN-PC-0LERV6)
Synonyms:
MDL No:
Molecular Formula: C12H14O
Molecular Weight: 174.2390

Identification/Properties

Properties
BP:
285.1°C at 760 mmHg
Storage:
Keep in dry area;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
174.243g/mol
XLogP3:
2.4
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
2
Exact Mass:
174.104g/mol
Monoisotopic Mass:
174.104g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
180
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:
H302-H315-H319-H335
Precautionary Statements:
P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-Benzylcyclopentanone, a versatile organic compound, plays a crucial role in chemical synthesis due to its unique structure and reactivity. In the realm of organic chemistry, this compound serves as a valuable building block for the synthesis of various pharmaceuticals, fragrances, and fine chemicals. Its cyclopentanone backbone contributes to its stability and compatibility with a wide range of reaction conditions.One of the key applications of 2-Benzylcyclopentanone is its use as a precursor in the synthesis of biologically active compounds. By undergoing various transformations, such as reduction, oxidation, or functional group modifications, this compound can be converted into structurally diverse molecules with potent biological activities. Its efficacy as a starting material in pharmaceutical synthesis makes it a sought-after compound in the pharmaceutical industry.Furthermore, 2-Benzylcyclopentanone's aromatic benzyl group imparts unique reactivity, allowing for selective functionalization at specific positions. This selective reactivity enables chemists to control the regiochemistry and stereochemistry of the final products, making it a valuable tool in complex molecule synthesis.Overall, the strategic placement of the benzyl group on the cyclopentanone scaffold makes 2-Benzylcyclopentanone a versatile and indispensable compound in chemical synthesis, facilitating the creation of diverse organic molecules with significant applications in various industries.