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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-Azetidinecarboxamide, N,N-dimethyl-, hydrochloride (1:1)

CN(C(=O)C1CNC1)C.Cl Request for Quotation
Chemical Name: 3-Azetidinecarboxamide, N,N-dimethyl-, hydrochloride (1:1)
CAS Number: 927390-60-1
Product Number: AG00IHB1(AGN-PC-09QAW6)
Synonyms:
MDL No:
Molecular Formula: C6H13ClN2O
Molecular Weight: 164.6332

Identification/Properties

Computed Properties
Molecular Weight:
164.633g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
164.072g/mol
Monoisotopic Mass:
164.072g/mol
Topological Polar Surface Area:
32.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
118
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302-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-Azetidinecarboxamide, N,N-dimethyl-, hydrochloride (1:1) is a versatile compound widely utilized in chemical synthesis as a key building block for the production of various pharmaceuticals, agrochemicals, and specialty chemicals. This compound serves as a valuable intermediate in the synthesis of complex organic compounds due to its unique chemical reactivity and structural properties.In chemical synthesis, 3-Azetidinecarboxamide, N,N-dimethyl-, hydrochloride (1:1) is often employed as a reactive intermediate in the formation of heterocyclic compounds and peptide derivatives. Its presence facilitates the intramolecular cyclization reactions necessary for the construction of diverse organic structures. Additionally, the hydrochloride salt form of this compound provides increased solubility and stability in certain reaction conditions, making it particularly useful for applications requiring aqueous environments or precise control over the reaction parameters.Furthermore, the incorporation of 3-Azetidinecarboxamide, N,N-dimethyl-, hydrochloride (1:1) in chemical synthesis processes enables chemists to access novel chemical scaffolds and functional groups that are essential for the development of advanced materials and bioactive molecules. By harnessing the reactivity and versatility of this compound, researchers can expedite the synthesis of complex chemical entities with defined stereochemistry and improved biological activity.Overall, the strategic use of 3-Azetidinecarboxamide, N,N-dimethyl-, hydrochloride (1:1) in chemical synthesis offers synthetic chemists a powerful tool for the efficient construction of diverse molecular architectures with potential applications across various industries.