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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-Azetidinecarboxylic acid, ethyl ester, hydrochloride

CCOC(=O)C1CNC1.Cl Request for Quotation
Chemical Name: 3-Azetidinecarboxylic acid, ethyl ester, hydrochloride
CAS Number: 405090-31-5
Product Number: AG00I7XW(AGN-PC-079RYI)
Synonyms:
MDL No:
Molecular Formula: C6H12ClNO2
Molecular Weight: 165.6180

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
165.617g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
3
Exact Mass:
165.056g/mol
Monoisotopic Mass:
165.056g/mol
Topological Polar Surface Area:
38.3A^2
Heavy Atom Count:
10
Formal Charge:
0
Complexity:
110
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


Ethyl azetidine-3-carboxylate hydrochloride, a versatile chemical compound, serves a crucial role in various chemical synthesis processes due to its unique properties. Commonly utilized as a key building block in the creation of complex organic molecules, this compound offers a valuable tool for chemists working in pharmaceutical, agrochemical, and material science industries.In chemical synthesis, Ethyl azetidine-3-carboxylate hydrochloride serves as a precursor in the preparation of diverse pharmacologically active compounds. Its reactivity and stability make it an ideal candidate for introducing specific functional groups or structural motifs into targeted molecules, enabling the efficient synthesis of novel drug candidates or pharmaceutical intermediates.Furthermore, the presence of the azetidine ring in Ethyl azetidine-3-carboxylate hydrochloride confers unique stereochemical properties that can be leveraged for the controlled synthesis of chiral compounds. This capability is particularly valuable in the development of enantiomerically pure substances, which are essential in medicinal chemistry and drug discovery to ensure optimal pharmacological activity and minimize potential side effects.Overall, Ethyl azetidine-3-carboxylate hydrochloride plays a vital role as a versatile synthetic building block, offering chemists a powerful tool for designing and preparing structurally diverse compounds with applications across various scientific fields.