
CAS 1064194-10-0
:1-Boc-3-bromo-azetidine
Description:
1-Boc-3-bromo-azetidine is a chemical compound characterized by its azetidine ring structure, which is a four-membered saturated heterocycle containing one nitrogen atom. The "Boc" (tert-butyloxycarbonyl) group is a common protecting group for amines, indicating that the nitrogen in the azetidine is substituted with this bulky group, enhancing the compound's stability and reactivity in synthetic applications. The presence of the bromine atom at the 3-position of the azetidine ring introduces a halogen functionality, which can be utilized in further chemical transformations, such as nucleophilic substitutions or coupling reactions. This compound is typically used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to serve as a building block for more complex molecules. Its properties, such as solubility and reactivity, can be influenced by the Boc group and the bromine substituent, making it a versatile intermediate in synthetic chemistry.
Formula:C8H14BrNO2
InChI:InChI=1S/C8H14BrNO2/c1-8(2,3)12-7(11)10-4-6(9)5-10/h6H,4-5H2,1-3H3
InChI key:RUTPPPNQDPSSBM-UHFFFAOYSA-N
SMILES:CC(C)(C)OC(=O)N1CC(C1)Br
Synonyms:- tert-Butyl 3-bromoazetidine-1-carboxylate
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tert-Butyl 3-bromoazetidine-1-carboxylate
CAS:Formula:C8H14BrNO2Purity:95%Color and Shape:LiquidMolecular weight:236.1091-Boc-3-bromoazetidine
CAS:1-Boc-3-bromoazetidineFormula:C8H14BrNO2Purity:>96%,stabilized with Na2S2O3Color and Shape:Colourless LiquidMolecular weight:236.10625tert-Butyl 3-bromoazetidine-1-carboxylate
CAS:Formula:C8H14BrNO2Purity:98%Color and Shape:LiquidMolecular weight:236.1063tert-Butyl 3-bromoazetidine-1-carboxylate
CAS:tert-Butyl 3-bromoazetidine-1-carboxylateFormula:C8H14BrNO2Purity:97%Molecular weight:236.11



