
CAS 1357943-15-7
:N-Boc-6-amino-3-chloro-2-fluoro-benzoic acid
Description:
N-Boc-6-amino-3-chloro-2-fluoro-benzoic acid is a chemical compound characterized by its specific functional groups and structural features. It contains a benzoic acid moiety with a chloro and a fluoro substituent at the 3 and 2 positions, respectively, and an amino group at the 6 position. The "N-Boc" designation indicates the presence of a tert-butyloxycarbonyl (Boc) protecting group on the amino group, which is commonly used in organic synthesis to temporarily protect amines. This compound is typically utilized in pharmaceutical research and development, particularly in the synthesis of biologically active molecules. Its properties include moderate solubility in organic solvents and potential reactivity due to the presence of the carboxylic acid and amino groups, making it a versatile intermediate in various chemical reactions. The presence of halogen atoms (chlorine and fluorine) can also influence its reactivity and biological activity, making it of interest in medicinal chemistry. Safety data and handling precautions should be observed due to its chemical nature.
Formula:C12H13ClFNO4
Synonyms:- Benzoic acid, 3-chloro-6-[[(1,1-dimethylethoxy)carbonyl]amino]-2-fluoro-
- N-Boc-6-amino-3-chloro-2-fluoro-benzoic acid
- 6-tert-Butoxycarbonylamino-3-chloro-2-fluoro-benzoic acid
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Found 2 products.
6-{[(tert-Butoxy)carbonyl]amino}-3-chloro-2-fluorobenzoic acid
CAS:<p>6-{[(tert-Butoxy)carbonyl]amino}-3-chloro-2-fluorobenzoic acid</p>Molecular weight:289.68732g/mol6-tert-Butoxycarbonylamino-3-chloro-2-fluoro-benzoic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C12H13ClFNO4Purity:Min. 95%Molecular weight:289.69 g/mol


