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· · COA & SDS available for every product · Same-day shipping on in-stock items Cinanserin hydrochloride - ≥95% , CAS No.54-84-2
Synonyms
AKOS037649253 | 2-Propenamide, N-[2-[[3-(dimethylamino)propyl]thio]phenyl]-3-phenyl-,monohydrochloride | Cinanserin HCl | Cinnamanilide, monohydrochloride | N-(2,6-Dimethylphenyl)-N-(phenylacetyl)-DL-alanine methyl ester | 1-beta,2-alpha-CHRYSENEDIOL, 1,2
Storage
Room temperature,Desiccated
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Why this grade ≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Room temperature,Desiccated Ships Normal Check lot-specific COA for exact specifications.
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Quality documents SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
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Literature proof Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Specifications Synonyms
AKOS037649253 | 2-Propenamide, N-[2-[[3-(dimethylamino)propyl]thio]phenyl]-3-phenyl-, monohydrochloride | Cinanserin HCl | Cinnamanilide, monohydrochloride | N-(2, 6-Dimethylphenyl)-N-(phenylacetyl)-DL-alanine methyl ester | 1-beta, 2-alpha-CHRYSENEDIOL, 1, 2
Specifications & Purity
≥95%
Biochemical and Physiological Mechanisms
5-HT2antagonist. Also inhibits 3C-like proteinase (3CLpro; Mpro). Inhibits replication of SARS-CoV.
Storage
Room temperature, Desiccated
Names and Identifiers Canonical Smiles CN(C)CCCSC1=CC=CC=C1NC(=O)C=CC2=CC=CC=C2.Cl IUPAC Name (E)-N-[2-[3-(dimethylamino)propylsulfanyl]phenyl]-3-phenylprop-2-enamide;hydrochloride InChIKey LXGJPDKYMJJWRB-IERUDJENSA-N INCHI 1S/C20H24N2OS.ClH/c1-22(2)15-8-16-24-19-12-7-6-11-18(19)21-20(23)14-13-17-9-4-3-5-10-17;/h3-7,9-14H,8,15-16H2,1-2H3,(H,21,23);1H/b14-13+; Isomeric SMILES CN(C)CCCSC1=CC=CC=C1NC(=O)/C=C/C2=CC=CC=C2.Cl Molecular Weight 376.94 Reaxy-Rn 7106997 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=7106997&ln=
Documentation 📋 Safety Data Sheet (SDS) Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS → ✅ Certificate of Analysis (COA) Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA → 📊 Datasheet Quick-reference summary of product specifications and applications.
View datasheet → 🔬 Specification Sheet Full quality attributes and acceptance criteria for this grade.
View spec sheet →
Advanced Data Taxonomic Classification Kingdom Organic compounds Superclass Phenylpropanoids and polyketides Class Cinnamic acids and derivatives Subclass Cinnamic acid amides Intermediate Tree Nodes Not available Direct Parent Cinnamic acid amides Alternative Parents Anilides Thiophenol ethers Styrenes N-arylamides Alkylarylthioethers Trialkylamines Secondary carboxylic acid amides Amino acids and derivatives Sulfenyl compounds Organopnictogen compounds Organic oxides Hydrochlorides Hydrocarbon derivatives Carbonyl compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Cinnamic acid amide - Anilide - Aryl thioether - Styrene - N-arylamide - Thiophenol ether - Alkylarylthioether - Monocyclic benzene moiety - Benzenoid - Amino acid or derivatives - Carboxamide group - Secondary carboxylic acid amide - Tertiary amine - Tertiary aliphatic amine - Carboxylic acid derivative - Sulfenyl compound - Thioether - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Amine - Organopnictogen compound - Carbonyl group - Organic oxygen compound - Hydrochloride - Organic nitrogen compound - Aromatic homomonocyclic compound Description This compound belongs to the class of organic compounds known as cinnamic acid amides. These are amides of cinnamic acids. Cinnamic acid is an aromatic compound containing a benzene and a carboxylic acid group forming 3-phenylprop-2-enoic acid. External Descriptors Not available Data sources 1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
3D Structure Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Solubility Solvent:water, Max Conc. mg/mL: None, Max Conc. mM: 50 Sensitivity Moisture sensitive. Molecular Weight 376.900 g/mol XLogP3 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 3 Rotatable Bond Count 8 Exact Mass 376.138 Da Monoisotopic Mass 376.138 Da Topological Polar Surface Area 57.600 Ų Heavy Atom Count 25 Formal Charge 0 Complexity 391.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 0 Undefined Atom Stereocenter Count 0 Defined Bond Stereocenter Count 1 Undefined Bond Stereocenter Count 0 The total count of all stereochemical bonds 1 Covalently-Bonded Unit Count 2
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