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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)-

methyl 3-aminoazetidine-1-carboxylate hydrochloride

COC(=O)N1CC(C1)N.Cl Request for Quotation
Chemical Name: methyl 3-aminoazetidine-1-carboxylate hydrochloride
CAS Number: 1803566-32-6
Product Number: AG01B156(AGN-PC-0WAJU9)
Synonyms:
MDL No:
Molecular Formula: C5H11ClN2O2
Molecular Weight: 166.6060

Identification/Properties

Computed Properties
Molecular Weight:
166.605g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
1
Exact Mass:
166.051g/mol
Monoisotopic Mass:
166.051g/mol
Topological Polar Surface Area:
55.6A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
120
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


Methyl 3-aminoazetidine-1-carboxylate hydrochloride, also known as MAAC hydrochloride, is a versatile compound widely used in chemical synthesis processes. This unique molecule serves as a key building block in the creation of pharmaceuticals, agrochemicals, and other fine chemicals. Its reactivity and functional groups make it an essential intermediate in organic synthesis. MAAC hydrochloride is particularly valued for its ability to participate in various chemical reactions, such as cyclizations, ring-opening reactions, and nucleophilic substitutions. Its structural properties allow for the strategic modification of molecules, leading to the synthesis of complex and diverse organic compounds with potential applications in drug discovery, material science, and beyond. By incorporating MAAC hydrochloride into synthetic pathways, chemists can access a wide range of structurally diverse compounds with enhanced properties and potential therapeutic benefits.