CAS 207799-10-8
:2-(Boc-amino)-4-bromopyridine
Description:
2-(Boc-amino)-4-bromopyridine is a chemical compound characterized by its pyridine ring, which is substituted at the 2-position with a tert-butyloxycarbonyl (Boc) protected amino group and at the 4-position with a bromine atom. The Boc group serves as a protective group for the amine, facilitating various synthetic applications by preventing unwanted reactions during chemical transformations. This compound is typically used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in nucleophilic substitution reactions and coupling reactions. It is a solid at room temperature and is generally handled under standard laboratory conditions. The presence of the bromine atom enhances its reactivity, making it a valuable intermediate in the synthesis of more complex molecules. As with many organic compounds, appropriate safety measures should be taken when handling this substance, including the use of personal protective equipment and adherence to safety data sheet guidelines.
Formula:C10H13BrN2O2
InChI:InChI=1/C10H13BrN2O2/c1-10(2,3)15-9(14)13-8-6-7(11)4-5-12-8/h4-6H,1-3H3,(H,12,13,14)
SMILES:CC(C)(C)OC(=Nc1cc(ccn1)Br)O
Synonyms:- tert-Butyl 4-bromopyridin-2-ylcarbamate
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Found 3 products.
Carbamic acid, N-(4-bromo-2-pyridinyl)-, 1,1-dimethylethyl ester
CAS:Formula:C10H13BrN2O2Purity:96%Color and Shape:SolidMolecular weight:273.1264tert-Butyl-4-bromo(pyridin-2-yl)carbamate
CAS:<p>tert-Butyl-4-bromo(pyridin-2-yl)carbamate</p>Purity:≥95%Color and Shape:SolidMolecular weight:273.13g/moltert-Butyl 4-Bromopyridin-2-ylcarbamate
CAS:Formula:C10H13BrN2O2Purity:96%Color and Shape:SolidMolecular weight:273.13


