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) |
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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.
| 정식 스마일 | Cc1csc(n1)[C@H]1CCCN1C(=O)c1cc(cc(c1)N(S(=O)(=O)C)C)C(=O)N[C@H]([C@@H](CNCc1cccc(c1)OC(F)(F)F)O)Cc1ccccc1 |
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| IUPAC Name | N-[(2S,3R)-3-hydroxy-1-phenyl-4-[[3-(trifluoromethoxy)phenyl]methylamino]butan-2-yl]-3-[methyl(methylsulfonyl)amino]-5-[(2R)-2-(4-methyl-1,3-thiazol-2-yl)pyrrolidine-1-carbonyl]benzamide |
| InChIKey | GUOONOJYWQOJJP-DCMFLLSESA-N |
| INCHI | 1S/C36H40F3N5O6S2/c1-23-22-51-34(41-23)31-13-8-14-44(31)35(47)27-17-26(18-28(19-27)43(2)52(3,48)49)33(46)42-30(16-24-9-5-4-6-10-24)32(45)21-40-20-25-11-7-12-29(15-25)50-36(37,38)39/h4-7,9-12,15,17-19,22,30-32,40,45H,8,13-14,16,20-21H2,1-3H3,(H,42,46)/t30-,31+,32+/m0/s1 |
| 이성체 SMILES | CC1=CSC(=N1)[C@H]2CCCN2C(=O)C3=CC(=CC(=C3)C(=O)N[C@@H](CC4=CC=CC=C4)[C@@H](CNCC5=CC(=CC=C5)OC(F)(F)F)O)N(C)S(=O)(=O)C |
| PubChem CID | 56846820 |
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 |
| 분류 | Benzene and substituted derivatives |
| Subclass | Phenylbutylamines |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Phenylbutylamines |
| Alternative Parents | Amphetamines and derivatives Sulfanilides Benzamides Benzoyl derivatives Benzylamines N-acylpyrrolidines Phenol ethers Phenoxy compounds Phenylmethylamines Aralkylamines 2,4-disubstituted thiazoles Organosulfonamides Organic sulfonamides Aminosulfonyl compounds Tertiary carboxylic acid amides Heteroaromatic compounds Tertiary amines Secondary carboxylic acid amides Secondary alcohols Trihalomethanes Amino acids and derivatives 1,2-aminoalcohols Azacyclic compounds Dialkylamines Organic oxides Alkyl fluorides Organofluorides Hydrocarbon derivatives |
| Molecular Framework | Aromatic heteromonocyclic compounds |
| Substituents | Phenylbutylamine - Amphetamine or derivatives - Sulfanilide - Benzamide - Benzoic acid or derivatives - Phenoxy compound - Benzoyl - Benzylamine - N-acylpyrrolidine - Phenol ether - Phenylmethylamine - Aralkylamine - 2,4-disubstituted 1,3-thiazole - Organosulfonic acid amide - Organic sulfonic acid amide - Aminosulfonyl compound - Thiazole - Tertiary carboxylic acid amide - Heteroaromatic compound - Sulfonyl - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Azole - Pyrrolidine - Tertiary amine - Trihalomethane - Amino acid or derivatives - Secondary carboxylic acid amide - 1,2-aminoalcohol - Carboxamide group - Secondary alcohol - Azacycle - Secondary amine - Organoheterocyclic compound - Secondary aliphatic amine - Carboxylic acid derivative - Halomethane - Alkyl fluoride - Alcohol - Organohalogen compound - Organic oxygen compound - Hydrocarbon derivative - Organofluoride - Organic nitrogen compound - Organonitrogen compound - Organooxygen compound - Organosulfur compound - Alkyl halide - Organic oxide - Amine - Aromatic heteromonocyclic compound |
| 설명 | This compound belongs to the class of organic compounds known as phenylbutylamines. These are compounds containing a phenylbutylamine moiety, which consists of a phenyl group substituted at the fourth carbon by an butan-1-amine. |
| External Descriptors | Not available |
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