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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-[2-(benzylamino)ethyl]carbamate;hydrochloride

O=C(OC(C)(C)C)NCCNCc1ccccc1.Cl Request for Quotation
Chemical Name: tert-butyl N-[2-(benzylamino)ethyl]carbamate;hydrochloride
CAS Number: 126402-64-0
Product Number: AG009X2E(AGN-PC-001D0V)
Synonyms:
MDL No:
Molecular Formula: C14H23ClN2O2
Molecular Weight: 286.7976

Identification/Properties

Computed Properties
Molecular Weight:
286.8g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
7
Exact Mass:
286.145g/mol
Monoisotopic Mass:
286.145g/mol
Topological Polar Surface Area:
50.4A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
243
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:
2
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


tert-Butyl (2-(benzylamino)ethyl)carbamate hydrochloride is a versatile reagent in chemical synthesis, commonly employed in the selective protection of primary and secondary amines. Its high reactivity and excellent stability make it an ideal choice for a wide range of applications in organic chemistry. By utilizing this compound, chemists can efficiently block specific amino groups in complex molecules, preventing undesired reactions and enabling precise control over the synthesis process. Additionally, tert-Butyl (2-(benzylamino)ethyl)carbamate hydrochloride can be easily removed under mild conditions, allowing for the ultimate flexibility in designing synthetic routes and functionalizing target molecules. Its role as a protecting group reagent highlights its importance in modern organic synthesis strategies, contributing to the development of novel compounds and materials with tailored properties.