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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 2-(aminomethyl)azetidine-1-carboxy...

NCC1CCN1C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-Butyl 2-(aminomethyl)azetidine-1-carboxy...
CAS Number: 939760-37-9
Product Number: AG0036VT(AGN-PC-0WAF5N)
Synonyms:
MDL No:
Molecular Formula: C9H18N2O2
Molecular Weight: 186.2514

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Liquid
Computed Properties
Molecular Weight:
186.255g/mol
XLogP3:
0.4
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
186.137g/mol
Monoisotopic Mass:
186.137g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
198
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


With its unique molecular structure, tert-Butyl 2-(aminomethyl)azetidine-1-carboxylate serves as a versatile building block in chemical synthesis. This compound offers a valuable tool for the efficient construction of complex molecules through strategic bond-forming reactions. By incorporating tert-Butyl 2-(aminomethyl)azetidine-1-carboxylate into synthetic pathways, chemists can access a wide range of functionalized derivatives and novel chemical entities. Its presence in the reaction sequence enables the introduction of diverse functionalities and stereochemical elements, providing opportunities for the creation of structurally diverse compounds with potential application in drug discovery, material science, and other research areas. Furthermore, the unique reactivity of tert-Butyl 2-(aminomethyl)azetidine-1-carboxylate allows for the rapid generation of molecular diversity, making it a valuable tool for the efficient and streamlined synthesis of target molecules with specific properties and biological activities.