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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)-

Acetic acid, (cyclopentyloxy)-

OC(=O)COC1CCCC1 Request for Quotation
Chemical Name: Acetic acid, (cyclopentyloxy)-
CAS Number: 95832-60-3
Product Number: AG0032VD(AGN-PC-00MBHU)
Synonyms:
MDL No: MFCD09930082
Molecular Formula: C7H12O3
Molecular Weight: 144.1684

Identification/Properties

Properties
BP:
291.52°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
144.17g/mol
XLogP3:
0.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
144.079g/mol
Monoisotopic Mass:
144.079g/mol
Topological Polar Surface Area:
46.5A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
116
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Cyclopentyloxy)acetic acid is a versatile compound commonly used in chemical synthesis for its unique properties. This compound serves as a valuable building block in the creation of various pharmaceuticals, agrochemicals, and specialty chemicals. Its cyclopentyloxy group provides steric hindrance, influencing the stereochemistry of reactions, making it particularly useful in asymmetric synthesis. Additionally, the carboxylic acid functionality of 2-(Cyclopentyloxy)acetic acid allows for easy derivatization, enabling the attachment of different functional groups to tailor the molecule's properties for specific applications in drug discovery and material science. By acting as a key intermediate, this compound plays a crucial role in the development of novel compounds with diverse applications across industries.