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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)-

1-AZETIDIN-3-YL-DIMETHYLAMINE HYDROCHLORIDE

CN(C1CNC1)C.Cl Request for Quotation
Chemical Name: 1-AZETIDIN-3-YL-DIMETHYLAMINE HYDROCHLORIDE
CAS Number: 935670-07-8
Product Number: AG00GUTV(AGN-PC-0W35NB)
Synonyms:
MDL No:
Molecular Formula: C5H13ClN2
Molecular Weight: 136.6231

Identification/Properties

Computed Properties
Molecular Weight:
136.623g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
136.077g/mol
Monoisotopic Mass:
136.077g/mol
Topological Polar Surface Area:
15.3A^2
Heavy Atom Count:
8
Formal Charge:
0
Complexity:
57.1
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#:
N/A
Hazard Statements:
H302-H315-H319-H335
Precautionary Statements:
P261-P280-P301+P312-P302+P352-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


N,N-Dimethylazetidin-3-amine hydrochloride, also known as $name$, is a versatile chemical compound widely used in chemical synthesis processes. This compound serves as an important intermediate in the preparation of various pharmaceuticals, agrochemicals, and functional materials. Its unique structure and reactivity make it a valuable building block for the creation of complex organic molecules.In chemical synthesis, N,N-Dimethylazetidin-3-amine hydrochloride acts as a key reagent in the formation of carbon-carbon and carbon-nitrogen bonds. Its presence enables the construction of intricate molecular frameworks through important reactions such as nucleophilic substitution, ring-closing metathesis, and palladium-catalyzed cross-coupling reactions. By facilitating these transformations, this compound plays a crucial role in the efficient and controlled assembly of target molecules with high chemical purity and yield.Moreover, N,N-Dimethylazetidin-3-amine hydrochloride exhibits excellent selectivity and compatibility with a wide range of functional groups, making it particularly valuable in the synthesis of complex natural products and pharmaceutical compounds. Its use as a versatile reagent in chemical transformations underscores its significance in advancing the field of organic chemistry and enabling the efficient production of novel and valuable molecules with diverse applications.