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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)-

3-(Cbz-Amino)-azetidine

O=C(NC1CNC1)OCc1ccccc1 Request for Quotation
Chemical Name: 3-(Cbz-Amino)-azetidine
CAS Number: 914348-04-2
Product Number: AG006AQT(AGN-PC-01LQXW)
Synonyms:
MDL No:
Molecular Formula: C11H14N2O2
Molecular Weight: 206.2411

Identification/Properties

Properties
Storage:
2-8℃;
Computed Properties
Molecular Weight:
206.245g/mol
XLogP3:
0.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
4
Exact Mass:
206.106g/mol
Monoisotopic Mass:
206.106g/mol
Topological Polar Surface Area:
50.4A^2
Heavy Atom Count:
15
Formal Charge:
0
Complexity:
211
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#:
N/A
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


3-(Cbz-Amino)-azetidine is a versatile compound widely utilized in chemical synthesis for the development of novel pharmaceuticals, agrochemicals, and materials. This unique molecule serves as a key building block for the construction of complex organic structures due to its reactivity and functional groups. In organic synthesis, 3-(Cbz-Amino)-azetidine is commonly employed as a nucleophile in various carbon-carbon and carbon-nitrogen bond-forming reactions. It plays a crucial role in the preparation of diverse pharmacologically active compounds by enabling the introduction of amino and carbonyl functionalities into target molecules. Additionally, the presence of a Cbz protecting group in 3-(Cbz-Amino)-azetidine ensures the selective manipulation of reactive sites during synthetic transformations, leading to enhanced control over regioselectivity and stereochemistry. This compound emerges as a valuable tool for chemists seeking to access structurally unique and biologically relevant molecules through strategic and efficient synthetic routes.