Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
Moligand™ Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships 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.
| Sorrisi canonici | COc1cc(ccc1O)N1CCN(CC1)CC(COc1ccccc1NC(=O)C)O |
|---|---|
| IUPAC Name | N-[2-[2-hydroxy-3-[4-(4-hydroxy-3-methoxyphenyl)piperazin-1-yl]propoxy]phenyl]acetamide |
| InChIKey | MXZGRDMOUWOERR-UHFFFAOYSA-N |
| INCHI | 1S/C22H29N3O5/c1-16(26)23-19-5-3-4-6-21(19)30-15-18(27)14-24-9-11-25(12-10-24)17-7-8-20(28)22(13-17)29-2/h3-8,13,18,27-28H,9-12,14-15H2,1-2H3,(H,23,26) |
| Isomeri SMILES | CC(=O)NC1=CC=CC=C1OCC(CN2CCN(CC2)C3=CC(=C(C=C3)O)OC)O |
| PubChem CID | 11429930 |
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 | Organoheterocyclic compounds |
| Classe | Diazinanes |
| Subclass | Piperazines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenylpiperazines |
| Alternative Parents | N-arylpiperazines Acetanilides Methoxyphenols Aminophenyl ethers Methoxyanilines N-acetylarylamines Phenoxy compounds p-Aminophenols Anisoles Dialkylarylamines Methoxybenzenes Alkyl aryl ethers N-alkylpiperazines 1-hydroxy-2-unsubstituted benzenoids Acetamides 1,2-aminoalcohols Amino acids and derivatives Secondary alcohols Secondary carboxylic acid amides Trialkylamines Azacyclic compounds Carbonyl compounds Organic oxides Hydrocarbon derivatives Organopnictogen compounds |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Phenylpiperazine - N-arylpiperazine - Methoxyphenol - Acetanilide - Aminophenyl ether - N-acetylarylamine - Methoxyaniline - Anilide - Aminophenol - Tertiary aliphatic/aromatic amine - Anisole - P-aminophenol - Phenol ether - Methoxybenzene - Aniline or substituted anilines - N-arylamide - Dialkylarylamine - Phenoxy compound - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Alkyl aryl ether - N-alkylpiperazine - Monocyclic benzene moiety - Benzenoid - Acetamide - 1,2-aminoalcohol - Amino acid or derivatives - Carboxamide group - Tertiary aliphatic amine - Tertiary amine - Secondary carboxylic acid amide - Secondary alcohol - Ether - Carboxylic acid derivative - Azacycle - Organic nitrogen compound - Carbonyl group - Hydrocarbon derivative - Organic oxide - Organonitrogen compound - Organooxygen compound - Amine - Alcohol - Organic oxygen compound - Organopnictogen compound - Aromatic heteromonocyclic compound |
| Descrizione | This compound belongs to the class of organic compounds known as phenylpiperazines. These are compounds containing a phenylpiperazine skeleton, which consists of a piperazine bound to a phenyl group. |
| External Descriptors | Not available |
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
|---|
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