N-Boc-5-Bromo-2-pyrimidinemethanamine is a chemical compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The "N-Boc" designation indicates the presence of a tert-butyloxycarbonyl (Boc) protecting group on the amine, which is commonly used in organic synthesis to protect amines during reactions. The compound also features a bromine atom at the 5-position of the pyrimidine ring, which can influence its reactivity and potential applications in medicinal chemistry. This compound is typically utilized in the synthesis of pharmaceuticals and agrochemicals, where the bromine substituent can serve as a site for further functionalization. Its solubility and stability can vary depending on the solvent and conditions used, making it important to consider these factors in practical applications. Overall, N-Boc-5-Bromo-2-pyrimidinemethanamine is a versatile intermediate in organic synthesis, particularly in the development of biologically active compounds.

N-Boc-5-Bromo-2-pyrimidinemethanamine

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tert-Butyl ((5-bromopyrimidin-2-yl)methyl)carbamate

CAS 1235451-38-3: N-Boc-5-Bromo-2-pyrimidinemethanamine

N-Boc-5-Bromo-2-pyrimidinemethanamine

Ref: 3D-FB156206

tert-Butyl ((5-bromopyrimidin-2-yl)methyl)carbamate

Ref: 54-OR82679

Carbamic acid, N-[(5-bromo-2-pyrimidinyl)methyl]-, 1,1-dimethylethyl ester

Ref: IN-DA000KRZ

N-Boc-5-Bromo-2-pyrimidinemethanamine

Ref: 10-F093610