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| 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.
| Canonical Smiles | COCCCNc1nc(Nc2nc(c(s2)C(=O)N2CCN(CC2)c2ncccn2)c2ccccc2)nc(n1)OC |
|---|---|
| IUPAC Name | 6-methoxy-N2-(3-methoxypropyl)-N4-{4-phenyl-5-[4-(pyrimidin-2-yl)piperazine-1-carbonyl]-1,3-thiazol-2-yl}-1,3,5-triazine-2,4-diamine |
| InChIKey | OIRCJRUZRVLDFA-UHFFFAOYSA-N |
| INCHI | 1S/C26H30N10O3S/c1-38-17-7-12-27-22-31-23(33-25(32-22)39-2)34-26-30-19(18-8-4-3-5-9-18)20(40-26)21(37)35-13-15-36(16-14-35)24-28-10-6-11-29-24/h3-6,8-11H,7,12-17H2,1-2H3,(H2,27,30,31,32,33,34) |
| Isomeric SMILES | COCCCNC1=NC(=NC(=N1)OC)NC2=NC(=C(S2)C(=O)N3CCN(CC3)C4=NC=CC=N4)C5=CC=CC=C5 |
| PubChem CID | 91938092 |
Comprehensive hazard, handling, storage, and regulatory compliance document.
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View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Diazinanes |
| Subclass | Piperazines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | N-arylpiperazines |
| Alternative Parents | Thiazolecarboxamides 1,3,5-triazine-2,4-diamines 2,4,5-trisubstituted thiazoles 2-heteroaryl carboxamides 2-methoxy-1,3,5-triazines Dialkylarylamines N-aliphatic s-triazines Alkyl aryl ethers Aminopyrimidines and derivatives 2-amino-1,3-thiazoles Benzene and substituted derivatives Heteroaromatic compounds Tertiary carboxylic acid amides Dialkyl ethers Azacyclic compounds Hydrocarbon derivatives Organic oxides |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | N-arylpiperazine - 2-heteroaryl carboxamide - 2,4,5-trisubstituted 1,3-thiazole - 2,4-diamine-s-triazine - 2-methoxy-1,3,5-triazine - Alkoxy-s-triazine - Thiazolecarboxamide - Thiazolecarboxylic acid or derivatives - Dialkylarylamine - Alkyl aryl ether - Aminopyrimidine - Amino-1,3,5-triazine - Aminotriazine - N-aliphatic s-triazine - Monocyclic benzene moiety - Pyrimidine - 1,3,5-triazine - Triazine - Benzenoid - 1,3-thiazol-2-amine - Thiazole - Tertiary carboxylic acid amide - Heteroaromatic compound - Azole - Carboxamide group - Dialkyl ether - Carboxylic acid derivative - Azacycle - Ether - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Amine - Organic oxygen compound - Aromatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as n-arylpiperazines. These are organic compounds containing a piperazine ring where the nitrogen ring atom carries an aryl group. |
| External Descriptors | Not available |
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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