CAS 66947-37-3
:N-(4-Bromo-2-methylphenyl)glycine
Description:
N-(4-Bromo-2-methylphenyl)glycine, with the CAS number 66947-37-3, is an organic compound characterized by its structure, which includes a glycine moiety attached to a 4-bromo-2-methylphenyl group. This compound typically exhibits properties associated with both amino acids and aromatic compounds. It is likely to be a white to off-white solid at room temperature, with moderate solubility in polar solvents such as water and alcohols, due to the presence of the amino and carboxylic acid functional groups. The bromine substituent on the aromatic ring can influence its reactivity and biological activity, potentially enhancing lipophilicity and affecting interactions with biological targets. As a derivative of glycine, it may participate in various biochemical processes and could be of interest in pharmaceutical research, particularly in the development of compounds with specific biological activities. Safety data should be consulted for handling and usage, as halogenated compounds can pose environmental and health risks.
Formula:C9H10BrNO2
InChI:InChI=1S/C9H10BrNO2/c1-6-4-7(10)2-3-8(6)11-5-9(12)13/h2-4,11H,5H2,1H3,(H,12,13)
InChI key:InChIKey=VLQCUVXTNBDRRF-UHFFFAOYSA-N
SMILES:N(CC(O)=O)C1=C(C)C=C(Br)C=C1
Synonyms:- Glycine, N-(4-bromo-o-tolyl)-
- N-(4-Bromo-2-methylphenyl)glycine
- Glycine, N-(4-bromo-2-methylphenyl)-
- 2-[(4-Bromo-2-methylphenyl)amino]acetic acid
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 1 products.
2-[(4-Bromo-2-methylphenyl)amino]acetic acid
CAS:<p>Versatile small molecule scaffold</p>Formula:C9H10BrNO2Purity:Min. 95%Molecular weight:244.08 g/mol
