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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 (trans-3-aminocyclopentyl)carbamate

N[C@H]1CC[C@@H](C1)NC(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-Butyl (trans-3-aminocyclopentyl)carbamate
CAS Number: 947732-58-3
Product Number: AG0039ZW(AGN-PC-0WB78H)
Synonyms:
MDL No:
Molecular Formula: C10H20N2O2
Molecular Weight: 200.2780

Identification/Properties

Computed Properties
Molecular Weight:
200.282g/mol
XLogP3:
1
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
200.152g/mol
Monoisotopic Mass:
200.152g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
211
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
2
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


$name$ is a versatile compound commonly used in chemical synthesis as a protecting group for amino acids during peptide synthesis. With its tert-butyl group strategically positioned, this molecule serves to temporarily shield the amine functional group in amino acids, preventing unwanted side reactions and ensuring selective reactivity in the desired steps of the synthetic pathway. By incorporating $name$ into the synthesis of peptides and other organic compounds, chemists can achieve precise control over the manipulation of amino acid residues, leading to higher yields and purer final products. This innovative application highlights the crucial role of $name$ in the advancement of modern organic chemistry techniques.