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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-(Methoxymethyl)azetidine hydrochloride

COCC1CNC1.Cl Request for Quotation
Chemical Name: 3-(Methoxymethyl)azetidine hydrochloride
CAS Number: 942308-06-7
Product Number: AG0065K7(AGN-PC-079RY2)
Synonyms:
MDL No:
Molecular Formula: C5H12ClNO
Molecular Weight: 137.6079

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
137.607g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
137.061g/mol
Monoisotopic Mass:
137.061g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
52
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


3-Methoxymethylazetidine hydrochloride is a versatile compound widely used in chemical synthesis for its unique properties and reactivity. As a key building block in organic chemistry, this compound serves as a valuable intermediate in the synthesis of various complex molecules and pharmaceuticals. Its methoxy and azetidine functional groups make it a valuable tool for introducing specific structural motifs into target molecules.One prominent application of 3-Methoxymethylazetidine hydrochloride is in the synthesis of heterocyclic compounds, where its azetidine ring can be efficiently incorporated into the molecular framework. This provides a valuable opportunity to modulate the physicochemical properties of the target molecules and enhance their biological activities. Furthermore, the methoxy group in 3-Methoxymethylazetidine hydrochloride can serve as a protecting group, allowing for selective transformations at other reactive sites within the molecule.In addition, 3-Methoxymethylazetidine hydrochloride is utilized in the preparation of chiral ligands and catalysts, where its structural features can impart stereochemical control in asymmetric reactions. Its versatility in chemical transformations makes it a valuable tool for synthetic chemists aiming to access diverse molecular architectures with high efficiency and selectivity.