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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)-

azetidin-3-amine;dihydrochloride

NC1CNC1.Cl.Cl Request for Quotation
Chemical Name: azetidin-3-amine;dihydrochloride
CAS Number: 102065-89-4
Product Number: AG0006HJ(AGN-PC-00MSDS)
Synonyms:
MDL No:
Molecular Formula: C3H10Cl2N2
Molecular Weight: 145.0309

Identification/Properties

Computed Properties
Molecular Weight:
145.027g/mol
Hydrogen Bond Donor Count:
4
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
144.022g/mol
Monoisotopic Mass:
144.022g/mol
Topological Polar Surface Area:
38A^2
Heavy Atom Count:
7
Formal Charge:
0
Complexity:
31.9
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:
3
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H302-H315-H319-H332-H335
Precautionary Statements:
P261-P280-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Azetidin-3-amine dihydrochloride is a versatile compound widely used in chemical synthesis. As a key building block in organic chemistry, it serves as a valuable intermediate for the preparation of various complex molecules. Its unique structure and reactivity make it a valuable tool for the creation of diverse chemical architectures.In synthetic chemistry, Azetidin-3-amine dihydrochloride is employed in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. It can be used in the construction of heterocyclic compounds, which are essential in the design and development of new drugs. The presence of the azetidine ring in its structure confers specific properties that can be harnessed for targeted synthetic routes.Additionally, Azetidin-3-amine dihydrochloride can participate in a variety of transformations, such as nucleophilic additions, cycloadditions, and ring-opening reactions. Its compatibility with a range of functional groups allows for versatility in synthetic strategies, enabling chemists to access a diverse array of compounds efficiently.Overall, the application of Azetidin-3-amine dihydrochloride in chemical synthesis plays a crucial role in the advancement of organic chemistry, enabling the construction of complex molecules with precision and efficiency.