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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-(Benzyloxy)azetidine, HCl

N1CC(C1)OCc1ccccc1.Cl Request for Quotation
Chemical Name: 3-(Benzyloxy)azetidine, HCl
CAS Number: 897019-59-9
Product Number: AG00IFSY(AGN-PC-0WA7J4)
Synonyms:
MDL No:
Molecular Formula: C10H14ClNO
Molecular Weight: 199.6773

Identification/Properties

Computed Properties
Molecular Weight:
199.678g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
3
Exact Mass:
199.076g/mol
Monoisotopic Mass:
199.076g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
13
Formal Charge:
0
Complexity:
128
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-(Benzyloxy)azetidine hydrochloride is a versatile chemical compound that finds extensive application in chemical synthesis. This compound is commonly used as a reagent in organic reactions due to its unique chemical properties. In chemical synthesis, 3-(Benzyloxy)azetidine hydrochloride serves as a valuable building block for creating complex molecules and structurally diverse compounds. Its presence allows for the efficient formation of new carbon-carbon and carbon-nitrogen bonds, making it an essential tool for the creation of pharmaceuticals, agrochemicals, and functional materials. Additionally, the incorporation of 3-(Benzyloxy)azetidine hydrochloride in synthesis routes enables chemists to access novel chemical structures that may not be easily attainable using traditional methods. By leveraging the reactivity and selectivity of this compound, researchers can streamline the synthesis of target molecules and accelerate the discovery of new chemical entities.