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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)-

2-(azetidin-3-yl)acetic acid;hydrochloride

OC(=O)CC1CNC1.Cl Request for Quotation
Chemical Name: 2-(azetidin-3-yl)acetic acid;hydrochloride
CAS Number: 952675-30-8
Product Number: AG00IIWQ(AGN-PC-0H1RYS)
Synonyms:
MDL No:
Molecular Formula: C5H10ClNO2
Molecular Weight: 151.5914

Identification/Properties

Computed Properties
Molecular Weight:
151.59g/mol
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
151.04g/mol
Monoisotopic Mass:
151.04g/mol
Topological Polar Surface Area:
49.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
98.6
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#:
-
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


2-(Azetidin-3-yl)acetic acid hydrochloride, also known as $name$, is a versatile compound widely used in chemical synthesis. This compound serves as a key building block in the creation of various pharmaceuticals, agrochemicals, and fine chemicals. In organic synthesis, $name$ plays a crucial role in the formation of diverse molecular structures due to its unique chemical properties. When utilized in chemical reactions, this compound facilitates the introduction of the azetidine ring, which is essential for enhancing the bioactivity and stability of the final products. Additionally, 2-(Azetidin-3-yl)acetic acid hydrochloride can be employed as a chiral auxiliary in asymmetric synthesis, enabling the selective formation of enantiomerically pure compounds. Its ability to participate in a wide range of chemical transformations makes it a valuable tool for researchers and chemists in the development of novel molecules with potential therapeutic or industrial applications.