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· · COA & SDS Disponible para cada producto · Same-day shipping on in-stock items 2-Iodo-5-nitrobenzoic acid - ≥98% , CAS No.19230-50-3
Synonyms
SCHEMBL3550116 | Benzoic acid, 2-iodo-5-nitro- | J-012426 | DS-16219 | SY040815 | 5-nitro-2-iodobenzoic acid | MFCD00234256 | JSSFIFUXHORXJX-UHFFFAOYSA-N | 2-iodo-5-nitro benzoic acid | 2-Iodo-5-nitrobenzoic acid | 2-iodo-5-nitro-benzoic acid | AKOS000149
Storage
Store at 2-8°C,Protected from light,Desiccated
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Why this grade ≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
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Storage & shipping Store at 2-8°C,Protected from light,Desiccated Ships Wet ice 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 Sinónimos
SCHEMBL3550116 | Benzoic acid, 2-iodo-5-nitro- | J-012426 | DS-16219 | SY040815 | 5-nitro-2-iodobenzoic acid | MFCD00234256 | JSSFIFUXHORXJX-UHFFFAOYSA-N | 2-iodo-5-nitro benzoic acid | 2-Iodo-5-nitrobenzoic acid | 2-iodo-5-nitro-benzoic acid | AKOS000149
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C, Protected from light, Desiccated
Enviado en
Wet ice
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Nombres e identificadores Sonrisas canónicas C1=CC(=C(C=C1[N+](=O)[O-])C(=O)O)I IUPAC Name 2-iodo-5-nitrobenzoic acid InChIKey JSSFIFUXHORXJX-UHFFFAOYSA-N INCHI 1S/C7H4INO4/c8-6-2-1-4(9(12)13)3-5(6)7(10)11/h1-3H,(H,10,11) Isómeros SMILES C1=CC(=C(C=C1[N+](=O)[O-])C(=O)O)I Peso molecular 293.02 Reaxy-Rn 2269455 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2269455&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 Benzenoids Clase Benzene and substituted derivatives Subclass Benzoic acids and derivatives Intermediate Tree Nodes Not available Direct Parent Nitrobenzoic acids and derivatives Alternative Parents 2-halobenzoic acids Halobenzoic acids Benzoic acids Nitrobenzenes 1-carboxy-2-haloaromatic compounds Benzoyl derivatives Nitroaromatic compounds Iodobenzenes Aryl iodides Vinylogous halides Monocarboxylic acids and derivatives Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organic oxides Organooxygen compounds Hydrocarbon derivatives Organopnictogen compounds Organoiodides Organonitrogen compounds Molecular Framework Aromatic homomonocyclic compounds Substituents Nitrobenzoate - 2-halobenzoic acid or derivatives - Halobenzoic acid or derivatives - 2-halobenzoic acid - Halobenzoic acid - Benzoic acid - Nitrobenzene - 1-carboxy-2-haloaromatic compound - Nitroaromatic compound - Benzoyl - Halobenzene - Iodobenzene - Aryl halide - Aryl iodide - Vinylogous halide - Organic nitro compound - C-nitro compound - Carboxylic acid derivative - Carboxylic acid - Organic 1,3-dipolar compound - Monocarboxylic acid or derivatives - Propargyl-type 1,3-dipolar organic compound - Allyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organopnictogen compound - Organic oxygen compound - Hydrocarbon derivative - Organic oxide - Organooxygen compound - Organohalogen compound - Organic nitrogen compound - Organoiodide - Organonitrogen compound - Aromatic homomonocyclic compound Descripción This compound belongs to the class of organic compounds known as nitrobenzoic acids and derivatives. These are compounds containing a nitrobenzoic acid moiety, which consists of a benzene ring bearing both a carboxylic acid group and a nitro group on two different ring carbon atoms. 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 Sensibilidad light sensitive Punto de ebullición (°C) 394.2°C at 760 mmHg Punto de fusión (°C) 197-198 °C Peso molecular 293.020 g/mol XLogP3 1.900 Hydrogen Bond Donor Count 1 Hydrogen Bond Acceptor Count 4 Rotatable Bond Count 1 Exact Mass 292.919 Da Monoisotopic Mass 292.919 Da Topological Polar Surface Area 83.100 Ų Heavy Atom Count 13 Formal Charge 0 Complexity 227.000 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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