| Cas No.: | 4424-17-3 |
| Chemical Name: | 2-Aminobenzanilide |
| Synonyms: | 2-Aminobenzanilide;2-Amino-N-phenylbenzamide~Phenylanthranilamide;2-Amino-N-phenylbenzamide;2-amino-N-phenyl-benzamide;amino-benzanilide;Anthranilanilide;Benzamide,2-amino-N-phenyl;Benzanilide,2-amino;EINECS 224-599-5;N1-phenyl-2-aminobenzamide;N-phenyl-2-aminobenzamide;N-Phenylanthranilamide |
| SMILES: | NC1C=CC=CC=1C(NC1C=CC=CC=1)=O |
| Formula: | C13H12N2O |
| M.Wt: | 212.247182846069 |
| Purity: | >98% |
| Sotrage: | 2 years -20°C Powder, 2 weeks 4°C in DMSO, 6 months -80°C in DMSO |
| Description: | 2-Aminobenzamide is a neutral and stable compound used as fluorescent tag, numerously in Glycan analysis. 2-aminobenzamide acts as the starting material for several important reactions like Bargellini reaction as an competent ambident nucleophile. Specifically 2-aminobenzamide and its derivatives are used in the blood coagulation cascade[1][2]. |
| References: | [1]. Pallavi More, et al. Natural surfactant mediated phytosynthesis and solvatochromic fluorescence of 2-aminobenzamide derivatives. RSC Adv., 2014,4, 63039-63047. |

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