Determine the necessary mass, volume, or concentration for preparing a solution.
≥97% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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.
| Canonical Smiles | C1CC(N(C1)CC2=CC=CC=C2)C(=O)[N-]C3=CC=CC=C3C(=NCC(=O)O)C4=CC=CC=C4.[Ni] |
|---|---|
| IUPAC Name | [(2S)-1-benzylpyrrolidine-2-carbonyl]-[2-[N-(carboxymethyl)-C-phenylcarbonimidoyl]phenyl]azanide;nickel |
| InChIKey | DRZQCPMTUIIOMU-JIDHJSLPSA-M |
| INCHI | 1S/C27H27N3O3.Ni/c31-25(32)18-28-26(21-12-5-2-6-13-21)22-14-7-8-15-23(22)29-27(33)24-16-9-17-30(24)19-20-10-3-1-4-11-20;/h1-8,10-15,24H,9,16-19H2,(H2,28,29,31,32,33);/p-1/t24-;/m0./s1 |
| Isomeric SMILES | C1C[C@H](N(C1)CC2=CC=CC=C2)C(=O)[N-]C3=CC=CC=C3C(=NCC(=O)O)C4=CC=CC=C4.[Ni] |
| PubChem CID | 11329479 |
| Molecular Weight | 498.208 |
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 | Benzenoids |
| Class | Benzene and substituted derivatives |
| Subclass | Diphenylmethanes |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Diphenylmethanes |
| Alternative Parents | Proline and derivatives Alpha amino acid amides Pyrrolidinecarboxamides Phenylmethylamines Benzylamines Aralkylamines N-alkylpyrrolidines Secondary ketimines Azomethines Trialkylamines Amino acids Organic transition metal salts Azacyclic compounds Monocarboxylic acids and derivatives Carbene-type 1,3-dipolar compounds Carboxylic acids Organic oxides Organopnictogen compounds Carbonyl compounds Hydrocarbon derivatives Organic anions |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Diphenylmethane - Proline or derivatives - Alpha-amino acid amide - Alpha-amino acid or derivatives - Benzylamine - Phenylmethylamine - Pyrrolidine carboxylic acid or derivatives - Pyrrolidine-2-carboxamide - Aralkylamine - N-alkylpyrrolidine - Azomethine - Pyrrolidine - Secondary ketimine - Amino acid or derivatives - Ketimine - Tertiary aliphatic amine - Tertiary amine - Amino acid - Organoheterocyclic compound - Carbene-type 1,3-dipolar compound - Carboxylic acid derivative - Carboxylic acid - Organic transition metal salt - Monocarboxylic acid or derivatives - Azacycle - Imine - Organic oxide - Organic salt - Carbonyl group - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Amine - Hydrocarbon derivative - Organopnictogen compound - Organic oxygen compound - Organic anion - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as diphenylmethanes. These are compounds containing a diphenylmethane moiety, which consists of a methane wherein two hydrogen atoms are replaced by two phenyl groups. |
| External Descriptors | Not available |