≥99% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C,Desiccated 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.
| Sonrisas canónicas | CC(=O)NC1=CC(=C(C=C1)O)SCC(C(=O)O)N.C(=O)(C(F)(F)F)O |
|---|---|
| IUPAC Name | (2R)-3-(5-acetamido-2-hydroxyphenyl)sulfanyl-2-aminopropanoic acid;2,2,2-trifluoroacetic acid |
| InChIKey | PDZGEXMJHANKLR-QRPNPIFTSA-N |
| INCHI | 1S/C11H14N2O4S.C2HF3O2/c1-6(14)13-7-2-3-9(15)10(4-7)18-5-8(12)11(16)17;3-2(4,5)1(6)7/h2-4,8,15H,5,12H2,1H3,(H,13,14)(H,16,17);(H,6,7)/t8-;/m0./s1 |
| Isómeros SMILES | CC(=O)NC1=CC(=C(C=C1)O)SC[C@@H](C(=O)O)N.C(=O)(C(F)(F)F)O |
| PubChem CID | 57350642 |
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 |
| Clase | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives - Alpha amino acids and derivatives - Cysteine and derivatives |
| Direct Parent | L-cysteine-S-conjugates |
| Alternative Parents | Acetanilides L-alpha-amino acids N-acetylarylamines Thiophenol ethers 1-hydroxy-2-unsubstituted benzenoids Alkylarylthioethers Alpha-halocarboxylic acids Acetamides Secondary carboxylic acid amides Amino acids Monocarboxylic acids and derivatives Carboxylic acids Sulfenyl compounds Monoalkylamines Hydrocarbon derivatives Carbonyl compounds Alkyl fluorides Organofluorides Organic oxides |
| Molecular Framework | Not available |
| Substituents | L-cysteine-s-conjugate - Alpha-amino acid - Acetanilide - L-alpha-amino acid - N-acetylarylamine - Anilide - Thiophenol ether - Aryl thioether - N-arylamide - 1-hydroxy-2-unsubstituted benzenoid - Phenol - Alkylarylthioether - Benzenoid - Monocyclic benzene moiety - Alpha-halocarboxylic acid - Acetamide - Alpha-halocarboxylic acid or derivatives - Amino acid - Carboxamide group - Secondary carboxylic acid amide - Sulfenyl compound - Thioether - Carboxylic acid - Monocarboxylic acid or derivatives - Organosulfur compound - Organofluoride - Organohalogen compound - Organonitrogen compound - Primary aliphatic amine - Organooxygen compound - Alkyl halide - Carbonyl group - Hydrocarbon derivative - Alkyl fluoride - Amine - Organic oxide - Organic oxygen compound - Primary amine - Organic nitrogen compound - Aromatic homomonocyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as l-cysteine-s-conjugates. These are compounds containing L-cysteine where the thio-group is conjugated. |
| External Descriptors | Not available |
| Peso molecular | 384.330 g/mol |
|---|---|
| XLogP3 | |
| Hydrogen Bond Donor Count | 5 |
| Hydrogen Bond Acceptor Count | 11 |
| Rotatable Bond Count | 5 |
| Exact Mass | 384.06 Da |
| Monoisotopic Mass | 384.06 Da |
| Topological Polar Surface Area | 175.000 Ų |
| Heavy Atom Count | 25 |
| Formal Charge | 0 |
| Complexity | 397.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 1 |
| 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 | 2 |
