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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, 2,4,4-trimethyl-

O=C1CC(CC1C)(C)C Request for Quotation
Chemical Name: Cyclopentanone, 2,4,4-trimethyl-
CAS Number: 4694-12-6
Product Number: AG003FLD(AGN-PC-0JLFUJ)
Synonyms:
MDL No:
Molecular Formula: C8H14O
Molecular Weight: 126.1962

Identification/Properties

Computed Properties
Molecular Weight:
126.199g/mol
XLogP3:
1.8
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
1
Rotatable Bond Count:
0
Exact Mass:
126.104g/mol
Monoisotopic Mass:
126.104g/mol
Topological Polar Surface Area:
17.1A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
136
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:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2,4,4-Trimethylcyclopentanone, often simply referred to as $name$, is a valuable compound widely used in chemical synthesis processes. This organic ketone plays a crucial role as a versatile building block in the creation of various chemical compounds.In chemical synthesis, 2,4,4-Trimethylcyclopentanone is commonly utilized as a key starting material for the production of pharmaceuticals, agrochemicals, fragrances, and advanced materials. Its unique chemical structure allows it to undergo selective reactions, contributing to the formation of more complex molecules with specific properties and functionalities.Due to its high reactivity and compatibility with different functional groups, $name$ serves as a critical intermediate in the synthesis of diverse organic compounds. Chemists leverage its structural features to introduce specific functional groups, modify molecular structures, and facilitate the formation of stereoisomers with desired characteristics.Furthermore, the use of 2,4,4-Trimethylcyclopentanone in chemical synthesis enables researchers to access new chemical entities, optimize reaction pathways, and enhance the efficiency of creating target molecules. Its importance in synthetic organic chemistry underscores its significance as a fundamental component in modern chemical research and development.In conclusion, the versatile application of 2,4,4-Trimethylcyclopentanone in chemical synthesis processes highlights its pivotal role in advancing diverse fields of science and technology.