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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-Boc-3-hydroxy-3-(aminomethyl)azetidine

NCC1(O)CN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: 1-Boc-3-hydroxy-3-(aminomethyl)azetidine
CAS Number: 1008526-71-3
Product Number: AG000308(AGN-PC-0WA4D2)
Synonyms:
MDL No:
Molecular Formula: C9H18N2O3
Molecular Weight: 202.2508

Identification/Properties

Computed Properties
Molecular Weight:
202.254g/mol
XLogP3:
-0.9
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
3
Exact Mass:
202.132g/mol
Monoisotopic Mass:
202.132g/mol
Topological Polar Surface Area:
75.8A^2
Heavy Atom Count:
14
Formal Charge:
0
Complexity:
229
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:
1
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

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Chemical Structure


The tert-Butyl 3-(aminomethyl)-3-hydroxyazetidine-1-carboxylate is a valuable compound used in chemical synthesis as a versatile building block. It serves as a crucial intermediate in the preparation of various pharmaceuticals and agrochemicals due to its unique structure. This compound plays a significant role in the construction of complex molecules by enabling the introduction of the important aminomethyl and hydroxy functionalities. Its reactivity and stability make it an excellent choice for creating structurally diverse organic compounds. In chemical synthesis, the tert-Butyl 3-(aminomethyl)-3-hydroxyazetidine-1-carboxylate acts as a key component in the production of advanced materials for various industrial applications.