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224,000+ productos de investigación · Triple ISO certified · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 6-Bromo-2-naphthyl β-D-glucuronide - ≥95% , CAS No.22720-35-0
Synonyms
6-BROMO-2-NAPHTHYL-BETA-D-GLUCURONIDE | 6-Bromo-2-naphthyl beta-D-glucopyranosiduronic acid | 6-Bromo-2-naphthyl beta -D-glucuronide | AKOS027381737 | AS-11181 | (2S,3S,4S,5R,6S)-6-(6-bromonaphthalen-2-yloxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxyl
Shipped In
Ice chest + Ice pads
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Why this grade ≥95% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at -20°C Ships Ice chest + Ice pads 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 6-Bromo-2-naphthyl β-D-glucuronide is a histochemical substrate for β-D-glucuronidase.
Specifications Sinónimos
6-BROMO-2-NAPHTHYL-BETA-D-GLUCURONIDE | 6-Bromo-2-naphthyl beta-D-glucopyranosiduronic acid | 6-Bromo-2-naphthyl beta -D-glucuronide | AKOS027381737 | AS-11181 | (2S,3S,4S,5R,6S)-6-(6-bromonaphthalen-2-yloxy)-3,4,5-trihydroxytetrahydro-2H-pyran-2-carboxyl
Especificaciones y pureza
≥95%
Condiciones de almacenamiento de almacenamiento
Store at -20°C
Enviado en
Ice chest + Ice pads
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Nombres e identificadores Sonrisas canónicas
C1=CC2=C(C=CC(=C2)Br)C=C1OC3C(C(C(C(O3)C(=O)O)O)O)O
IUPAC Name
(2S,3S,4S,5R,6S)-6-(6-bromonaphthalen-2-yl)oxy-3,4,5-trihydroxyoxane-2-carboxylic acid
InChIKey
TYDGGWYIJKMLEO-JHZZJYKESA-N
INCHI
1S/C16H15BrO7/c17-9-3-1-8-6-10(4-2-7(8)5-9)23-16-13(20)11(18)12(19)14(24-16)15(21)22/h1-6,11-14,16,18-20H,(H,21,22)/t11-,12-,13+,14-,16+/m0/s1
Isómeros SMILES
C1=CC2=C(C=CC(=C2)Br)C=C1O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)C(=O)O)O)O)O
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 Organic oxygen compounds Clase Organooxygen compounds Subclass Carbohydrates and carbohydrate conjugates Intermediate Tree Nodes Glycosyl compounds Direct Parent Phenolic glycosides Alternative Parents O-glucuronides Hexoses O-glycosyl compounds Naphthalenes Beta hydroxy acids and derivatives Pyrans Aryl bromides Oxanes Secondary alcohols Acetals Polyols Oxacyclic compounds Carboxylic acids Monocarboxylic acids and derivatives Organobromides Hydrocarbon derivatives Carbonyl compounds Organic oxides Molecular Framework Aromatic heteropolycyclic compounds Substituents Phenolic glycoside - 1-o-glucuronide - O-glucuronide - Glucuronic acid or derivatives - Hexose monosaccharide - O-glycosyl compound - Naphthalene - Beta-hydroxy acid - Aryl bromide - Aryl halide - Hydroxy acid - Monosaccharide - Benzenoid - Pyran - Oxane - Secondary alcohol - Organoheterocyclic compound - Acetal - Monocarboxylic acid or derivatives - Oxacycle - Carboxylic acid - Carboxylic acid derivative - Polyol - Hydrocarbon derivative - Alcohol - Organic oxide - Organohalogen compound - Organobromide - Carbonyl group - Aromatic heteropolycyclic compound Descripción This compound belongs to the class of organic compounds known as phenolic glycosides. These are organic compounds containing a phenolic structure attached to a glycosyl moiety. Some examples of phenolic structures include lignans, and flavonoids. Among the sugar units found in natural glycosides are D-glucose, L-Fructose, and L rhamnose. 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 Certificados (CoA, COO, BSE/TSE y tabla de análisis) Propiedades químicas y físicas Peso molecular 399.190 g/mol XLogP3 2.000 Hydrogen Bond Donor Count 4 Hydrogen Bond Acceptor Count 7 Rotatable Bond Count 3 Exact Mass 398 Da Monoisotopic Mass 398 Da Topological Polar Surface Area 116.000 Ų Heavy Atom Count 24 Formal Charge 0 Complexity 462.000 Isotope Atom Count 0 Defined Atom Stereocenter Count 5 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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