Rhodanine - ≥99%(HPLC), for garlic acid determination by spectrum , CAS No.141-84-4

Name: Rhodanine - ≥99%(HPLC), for garlic acid determination by spectrum , CAS No.141-84-4
Brand: Aladdin Scientific
SKU: R104133
Availability: InStock

CAS: 141-84-4 Cat. No.: R104133 Peso molecular: 133.19 Beilstein Registry Number: 110701 Número EC: 205-505-1 PubChem CID: 1201546

6 Citations COA

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Rhodanine - ≥99%(HPLC), for garlic acid determination by spectrum CAS No(141-84-4) by Aladdin Scientific

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Disponible para pedir

GRADE & PURITY ≥99%(HPLC) for garlic acid determination by spectrum

Synonyms

Storage

Room temperature

Shipped In

Normal

Specifications Nombres e identificadores Documentation Advanced Data Taxonomic Classification Estructura 3D Objetivos asociados (humanos) Objetivos asociados (no humanos) Mecanismos de acción Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Preguntas frecuentes y artículos Citations of This Product Referencias Calculadoras de soluciones Reseñas

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Why this grade

≥99%(HPLC), for garlic acid determination by spectrum for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

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Storage & shipping

Room temperature 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 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos

Especificaciones y pureza

≥99%(HPLC), for garlic acid determination by spectrum

Mecanismos bioquímicos y fisiológicos

Auguste Rodin was able to inhibit the replication of Echo virus 12 and the development of virus-induced morphological changes.

Condiciones de almacenamiento de almacenamiento

Room temperature

Enviado en

Normal

Pureza

≥99%(HPLC)

Nombres e identificadores

Pubchem Sid	504760412
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/504760412
Sonrisas canónicas	C1C(=O)NC(=S)S1
IUPAC Name	2-sulfanylidene-1,3-thiazolidin-4-one
InChIKey	KIWUVOGUEXMXSV-UHFFFAOYSA-N
INCHI	1S/C3H3NOS2/c5-2-1-7-3(6)4-2/h1H2,(H,4,5,6)
Isómeros SMILES	C1C(=O)NC(=S)S1
WGK Alemania	3
RTECS	VI7700000
PubChem CID	1201546
Peso molecular	133.19
Beilstein	110701

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

Taxonomy Tree

Kingdom Organic compounds
- Superclass Organoheterocyclic compounds
  - Clase Azolidines
    - Subclass Thiazolidines

Kingdom	Organic compounds
Superclass	Organoheterocyclic compounds
Clase	Azolidines
Subclass	Thiazolidines
Intermediate Tree Nodes	Not available
Direct Parent	Thiazolidinethiones
Alternative Parents	Cyclic dithiocarbamic acid esters Carboxylic acids and derivatives Azacyclic compounds Organosulfur compounds Organopnictogen compounds Organonitrogen compounds Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic heteromonocyclic compounds
Substituents	Thiazolidinethione - Cyclic dithiocarbamic acid ester - Dithiocarbamic acid ester - Azacycle - Carboxylic acid derivative - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organosulfur compound - Organooxygen compound - Organonitrogen compound - Carbonyl group - Aliphatic heteromonocyclic compound
Descripción	This compound belongs to the class of organic compounds known as thiazolidinethiones. These are heterocyclic compounds containing a thiazolidinethione ring which bears one thioketone group.
External Descriptors	thiazolidinone
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. DOI: 10.1186/s13321-016-0174-y

Estructura 3D

Objetivos asociados (humanos)

F2 Tclin Thrombin (11687 Activities)

Discover Target: F2

Activity Type	Relation	Activity value	Units	Action Type	Journal	PubMed Id	doi	Assay Aladdin ID

ACHN (49357 Activities)

Lot Number	Certificate Type	Fecha	Articulo
A2620002	Certificate of Analysis	Jan 22, 2026	R104133
D23261198	Certificate of Analysis	May 18, 2023	R104133
J2231150	Certificate of Analysis	May 18, 2023	R104133
J2231152	Certificate of Analysis	May 18, 2023	R104133
J2231153	Certificate of Analysis	May 18, 2023	R104133

Solubilidad	Soluble in water (2.25 g/L at 20°C).
Sensibilidad	Moisture sensitive.
Punto de fusión (°C)	165-169°C
Peso molecular	133.200 g/mol
XLogP3	0.700
Hydrogen Bond Donor Count	1
Hydrogen Bond Acceptor Count	3
Rotatable Bond Count	0
Exact Mass	132.966 Da
Monoisotopic Mass	132.966 Da
Topological Polar Surface Area	86.500 Å²
Heavy Atom Count	7
Formal Charge	0
Complexity	122.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	0
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	1