1. Home
  2. 3-propan-2-yloxyazetidine;hydrochloride

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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-propan-2-yloxyazetidine;hydrochloride

CC(OC1CNC1)C.Cl Request for Quotation
Chemical Name: 3-propan-2-yloxyazetidine;hydrochloride
CAS Number: 871657-49-7
Product Number: AG003JM3(AGN-PC-09OFQX)
Synonyms:
MDL No:
Molecular Formula: C6H14ClNO
Molecular Weight: 151.6345

Identification/Properties

Properties
Storage:
Inert atmosphere;2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
151.634g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
2
Exact Mass:
151.076g/mol
Monoisotopic Mass:
151.076g/mol
Topological Polar Surface Area:
21.3A^2
Heavy Atom Count:
9
Formal Charge:
0
Complexity:
68.9
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:
2
Compound Is Canonicalized:
Yes

Safety Information

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

NMR Spectrum

Other Analytical Data

Request for Quotation

Customer Feedback

Chemical Structure


Azetidine, 3-(1-methylethoxy)-, hydrochloride (1:1) is a valuable chemical reagent commonly used in chemical synthesis due to its versatile applications. This compound is utilized in various organic transformations to introduce the azetidine ring into molecular structures, offering unique three-dimensional geometries and enhanced reactivity profiles. In particular, the hydrochloride salt form of this compound serves as an important intermediate in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its selective reactivity and compatibility with a wide range of functional groups make it a preferred choice for conducting complex synthetic procedures, such as ring-opening reactions, cyclization reactions, and N-functionalization processes. Moreover, the presence of the methylethoxy group provides additional steric and electronic effects, allowing for the fine-tuning of reaction pathways and product yields. In summary, Azetidine, 3-(1-methylethoxy)-, hydrochloride (1:1) plays a crucial role in modern organic synthesis by enabling the construction of diverse molecular architectures with enhanced biological and chemical properties.