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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)-

2-cyclopentyloxyethanamine

NCCOC1CCCC1 Request for Quotation
Chemical Name: 2-cyclopentyloxyethanamine
CAS Number: 933732-12-8
Product Number: AG003F0X(AGN-PC-01619U)
Synonyms:
MDL No: MFCD09730285
Molecular Formula: C7H15NO
Molecular Weight: 129.2001

Identification/Properties

Properties
BP:
201.8°C at 760 mmHg
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
129.203g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
129.115g/mol
Monoisotopic Mass:
129.115g/mol
Topological Polar Surface Area:
35.2A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
69.3
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:
Danger
UN#:
2735
Hazard Statements:
H314
Precautionary Statements:
P280-P305+P351+P338-P310
Class:
8
Packing Group:
Ⅲ

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Cyclopentyloxy)ethylamine is a versatile compound that finds application in various chemical synthesis processes. As a primary amine, it serves as a valuable building block in the production of pharmaceuticals, agrochemicals, and other fine chemicals. The presence of the cyclopentyl group offers unique steric and electronic properties that can be exploited to control reactivity and selectivity in reactions.In organic synthesis, 2-(Cyclopentyloxy)ethylamine can be used as a nucleophilic reagent in the formation of amides, esters, and other functional groups. Its primary amine functionality allows for direct amidation reactions with carboxylic acids, providing a straightforward route to amide derivatives. Additionally, the cyclopentyl ether moiety can be selectively deprotected under mild conditions, enabling further manipulation of the molecule.Furthermore, 2-(Cyclopentyloxy)ethylamine can be employed in the synthesis of heterocyclic compounds, such as aziridines and oxazolidines, through ring-closure reactions. The cyclopentyl group can influence the regioselectivity and diastereoselectivity of these transformations, leading to the formation of complex molecular structures with high efficiency.Overall, the strategic incorporation of 2-(Cyclopentyloxy)ethylamine in chemical synthesis offers chemists a valuable tool for the construction of diverse organic molecules with tailored properties and functionalities.