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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)-

tert-butyl N-[(1R)-2-amino-1-cyclopentylethyl]carbamate

NCC(C1CCCC1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-butyl N-[(1R)-2-amino-1-cyclopentylethyl]carbamate
CAS Number: 936497-76-6
Product Number: AG00GSM3(AGN-PC-059AX2)
Synonyms:
MDL No:
Molecular Formula: C12H24N2O2
Molecular Weight: 228.3312

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
228.336g/mol
XLogP3:
1.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
5
Exact Mass:
228.184g/mol
Monoisotopic Mass:
228.184g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
16
Formal Charge:
0
Complexity:
230
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-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Tert-Butyl (2-amino-1-cyclopentylethyl)carbamate is a versatile compound commonly utilized in chemical synthesis for its unique properties and reactivity. This compound serves as a valuable building block in the creation of various organic molecules and pharmaceuticals due to its stability and compatibility with a wide range of reaction conditions. In chemical synthesis, tert-Butyl (2-amino-1-cyclopentylethyl)carbamate can be selectively deprotected to expose the amine functionality, enabling further derivatization and incorporation into more complex molecular structures. Additionally, its sterically hindered tert-butyl group provides protection to the amine moiety, allowing for controlled reactions and the formation of desired products with high yield and purity. This compound plays a crucial role in the development of novel compounds and the advancement of synthetic strategies in organic chemistry.