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· · COA & SDS Disponível para todos os produtos · Envio no mesmo dia em itens em estoque 6-Bromo-2-naphthyl β-D-glucuronide - ≥95% , CAS No.22720-35-0
Disponível para encomenda
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.
Visão geral 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
Especificações e pureza
≥95%
Condições de armazenamento de armazenamento
Store at -20°C
Enviado em
Ice chest + Ice pads
Este produto requer transporte de cadeia fria. Serviços terrestres e outros serviços econômicos não estão disponíveis.
Nomes e identificadores Sorrisos canónicos
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
SMILES isoméricas
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 Classe 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 Descrição 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.
Estrutura 3D Certificados（CoA,COO,BSE/TSE e Mapa de Análise) Propriedades químicas e 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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