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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 5-amino-1,3,4-tiadiazol-2-sulfonamida - Moligand™, ≥97% , CAS No.14949-00-9
GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥97% Synonyms
F11831 | J-008594 | 1,3,4-Thiadiazole-2-sulfonamide, 5-amino- (8CI)(9CI) | AS-47063 | DESACETYL ACETAZOLAMIDE [USP IMPURITY] | AKOS006228258 | alpha-Phenyl-2-pyridinemethanol | BCP33816 | 5-Amino-1,3,4-thiadiazole-2-sulfonamide | SY260062 | 1-phenylsulfon
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Why this grade Moligand™, ≥97% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Conservar a 2-8°C Ships Hielo húmedo 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.
Descripción general la 5-amino-1,3,4-tiadiazol-2-sulfonamida es una acetazolamida intermedia.
Specifications Sinónimos
F11831 | J-008594 | 1, 3, 4-Thiadiazole-2-sulfonamide, 5-amino- (8CI)(9CI) | AS-47063 | DESACETYL ACETAZOLAMIDE [USP IMPURITY] | AKOS006228258 | alpha-Phenyl-2-pyridinemethanol | BCP33816 | 5-Amino-1, 3, 4-thiadiazole-2-sulfonamide | SY260062 | 1-phenylsulfon
Especificaciones y pureza
Moligand™, ≥97%
Condiciones de almacenamiento de almacenamiento
Conservar a 2-8°C
Propiedades del producto pKa pKa: 7.76 (Predicted) Datos Ki CA VII: Ki= 5.2 nM (human); CA XII: Ki= 33 nM (human); CA IX: Ki= 41 nM (human); Carbonic anhydrase 15: Ki= 48 nM (mouse); CA II: Ki= 60 nM (human)
Nombres e identificadores Sonrisas canónicas C1(=NN=C(S1)S(=O)(=O)N)N IUPAC Name 5-amino-1,3,4-thiadiazole-2-sulfonamide InChIKey VGMVBPQOACUDRU-UHFFFAOYSA-N INCHI 1S/C2H4N4O2S2/c3-1-5-6-2(9-1)10(4,7)8/h(H2,3,5)(H2,4,7,8) Isómeros SMILES C1(=NN=C(S1)S(=O)(=O)N)N Peso molecular 180.21 Reaxy-Rn 149685 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=149685&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 Organoheterocyclic compounds Clase Azoles Subclass Thiadiazoles Intermediate Tree Nodes Not available Direct Parent Thiadiazole sulfonamides Alternative Parents 2-amino-5-substituted-1,3,4-thiadiazoles Organosulfonamides Heteroaromatic compounds Aminosulfonyl compounds Azacyclic compounds Primary amines Organopnictogen compounds Organic oxides Hydrocarbon derivatives Molecular Framework Aromatic heteromonocyclic compounds Substituents 1,3,4-thiadiazole-2-sulfonamide - 2-amino-5-substituted-1,3,4-thiadiazole - 2-amino-1,3,4-thiadiazole - Organosulfonic acid amide - Organic sulfonic acid or derivatives - Organosulfonic acid or derivatives - Sulfonyl - Heteroaromatic compound - Aminosulfonyl compound - Azacycle - Amine - Hydrocarbon derivative - Organic oxide - Organopnictogen compound - Organic oxygen compound - Primary amine - Organosulfur compound - Organonitrogen compound - Organic nitrogen compound - Aromatic heteromonocyclic compound Descripción This compound belongs to the class of organic compounds known as thiadiazole sulfonamides. These are heterocyclic compounds containing a thiazole ring substituted by at least one sulfonamide group. 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.
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 Solubilidad Soluble in DMSO, and methanol. Sensibilidad Air sensitive Índice de refracción n20D1.68 (Predicted) Punto de ebullición (°C) ~484.2° C at 760 mmHg (Predicted) Punto de fusión (°C) 188-190° C (dec.) Peso molecular 180.210 g/mol XLogP3 -0.900 Hydrogen Bond Donor Count 2 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 1 Exact Mass 179.978 Da Monoisotopic Mass 179.978 Da Topological Polar Surface Area 149.000 Ų Heavy Atom Count 10 Formal Charge 0 Complexity 208.000 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
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