NC1=CC=CC=C1NC(=O)\C=C\C1=CC=C(C=C1)C(N1CCC(O)C1)C(=O)NC1=CC=C(Br)C=C1

InChIKey=VQHGQDXRCOYKQH-VGOFMYFVSA-N

C27H27BrN4O3

535.442

Organic compounds

Organic acids and derivatives

Carboxylic acids and derivatives

Amino acids, peptides, and analogues

Amino acids and derivatives - Alpha amino acids and derivatives

Alpha amino acid amides

Cinnamic acid amides Phenylacetamides 2'-Aminoanilides Styrenes Aniline and substituted anilines N-arylamides Aralkylamines Bromobenzenes N-alkylpyrrolidines Aryl bromides Trialkylamines Secondary carboxylic acid amides Secondary alcohols 1,2-aminoalcohols Azacyclic compounds Carbonyl compounds Hydrocarbon derivatives Organic oxides Organobromides Primary amines

Aromatic heteromonocyclic compounds

Alpha-amino acid amide - Cinnamic acid or derivatives - Cinnamic acid amide - 2'-aminoanilide - Phenylacetamide - Anilide - Styrene - N-arylamide - Aniline or substituted anilines - Halobenzene - Bromobenzene - Aralkylamine - Aryl bromide - Monocyclic benzene moiety - N-alkylpyrrolidine - Benzenoid - Aryl halide - Pyrrolidine - Secondary alcohol - 1,2-aminoalcohol - Secondary carboxylic acid amide - Carboxamide group - Tertiary aliphatic amine - Tertiary amine - Azacycle - Organoheterocyclic compound - Primary amine - Organohalogen compound - Organobromide - Organonitrogen compound - Carbonyl group - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Amine - Organic nitrogen compound - Alcohol - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids.

Not available