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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-[(1-aminocyclopropyl)methyl]carbamate

O=C(OC(C)(C)C)NCC1(N)CC1 Request for Quotation
Chemical Name: tert-butyl N-[(1-aminocyclopropyl)methyl]carbamate
CAS Number: 934481-48-8
Product Number: AG00H0ZD(AGN-PC-0HY69V)
Synonyms:
MDL No:
Molecular Formula: C9H18N2O2
Molecular Weight: 186.2514

Identification/Properties

Computed Properties
Molecular Weight:
186.255g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
186.137g/mol
Monoisotopic Mass:
186.137g/mol
Topological Polar Surface Area:
64.4A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
204
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#:
-
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


The tert-Butyl ((1-aminocyclopropyl)methyl)carbamate is a versatile chemical compound widely used in chemical synthesis. In organic chemistry, this compound serves as a valuable building block for the preparation of various complex molecules and pharmaceuticals. Its unique structure provides opportunities for creating new carbon-carbon bonds and introducing functional groups with precision. With its stability and reactivity under controlled conditions, tert-Butyl ((1-aminocyclopropyl)methyl)carbamate can be selectively modified to tailor its properties for specific synthetic pathways. Additionally, its presence can enhance the overall efficiency and selectivity of multi-step synthesis processes. This compound's utility extends to the synthesis of bioactive compounds, natural products, and materials with potential applications across different industries.