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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)-

tert-Butyl 3-ethyl-3-(hydroxymethyl)azetidine-1-carboxylate

CCC1(CO)CN(C1)C(=O)OC(C)(C)C Request for Quotation
Chemical Name: tert-Butyl 3-ethyl-3-(hydroxymethyl)azetidine-1-carboxylate
CAS Number: 1638761-21-3
Product Number: AG001UHF(AGN-PC-0WCJYP)
Synonyms:
MDL No: MFCD27986956
Molecular Formula: C11H21NO3
Molecular Weight: 215.2893

Identification/Properties

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


The tert-butyl 3-ethyl-3-(hydroxymethyl)azetidine-1-carboxylate is a versatile compound widely used in chemical synthesis due to its unique chemical properties. This compound serves as a valuable building block in the preparation of various organic molecules and pharmaceuticals. Its azetidine moiety assists in the formation of diverse ring structures, making it crucial in the synthesis of complex organic compounds. With its tert-butyl and hydroxymethyl groups, this compound enables the introduction of bulky and functionalized substituents, enhancing the diversity and reactivity of the synthesized products. In addition, the presence of the ethyl group provides flexibility in molecular design, allowing for the modification of stereochemistry and overall molecular conformation. Overall, tert-butyl 3-ethyl-3-(hydroxymethyl)azetidine-1-carboxylate plays a significant role in advancing chemical synthesis strategies and expanding the scope of organic chemistry research.