≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
2-Anilinoacetamide is used as an initial substrate for the enzymic synthesis of Cephalexin with liquid penicillin G acylase.
| Pubchem Sid | 504767838 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504767838 |
| Sorrisi canonici | C1=CC=C(C=C1)NCC(=O)N |
| IUPAC Name | 2-anilinoacetamide |
| InChIKey | GXBRYTMUEZNYJT-UHFFFAOYSA-N |
| INCHI | 1S/C8H10N2O/c9-8(11)6-10-7-4-2-1-3-5-7/h1-5,10H,6H2,(H2,9,11) |
| Isomeri SMILES | C1=CC=C(C=C1)NCC(=O)N |
| Peso molecolare | 150.18 |
| Reaxy-Rn | 2086741 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2086741&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic acids and derivatives |
| Classe | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives |
| Direct Parent | Alpha amino acid amides |
| Alternative Parents | Phenylalkylamines Aniline and substituted anilines Secondary alkylarylamines Primary carboxylic acid amides Organopnictogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds |
| Molecular Framework | Aromatic homomonocyclic compounds |
| Substituents | Alpha-amino acid amide - Aniline or substituted anilines - Phenylalkylamine - Secondary aliphatic/aromatic amine - Benzenoid - Monocyclic benzene moiety - Primary carboxylic acid amide - Carboxamide group - Secondary amine - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Amine - Organic oxide - Aromatic homomonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as alpha amino acid amides. These are amide derivatives of alpha amino acids. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Data | Oggetto |
|---|---|---|---|
 E2621230 | Certificate of Analysis | May 28, 2026 | A357212 |
| A2207346 | Certificate of Analysis | Oct 22, 2024 | A357212 |
| A2207365 | Certificate of Analysis | Oct 22, 2024 | A357212 |
| A2207366 | Certificate of Analysis | Oct 22, 2024 | A357212 |
| A2207435 | Certificate of Analysis | Oct 22, 2024 | A357212 |
| Indice di rifrazione | n20D1.62 (Predicted) |
|---|---|
| Punto di infiammabilità (°C) | 187.102°C |
| Punto di ebollizione (°C) | 385.76° C at 760 mmHg (Predicted) |
| Punto di fusione (°C) | 114.75° C (Predicted) |
| Peso molecolare | 150.180 g/mol |
| XLogP3 | 0.000 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 3 |
| Exact Mass | 150.079 Da |
| Monoisotopic Mass | 150.079 Da |
| Topological Polar Surface Area | 55.100 Ų |
| Heavy Atom Count | 11 |
| Formal Charge | 0 |
| Complexity | 130.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
