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· · COA & SDS available for every product · Same-day shipping on in-stock items Bromonitromethane - ≥90% , CAS No.563-70-2
Synonyms
1-bromonitromethane | EG63P9EUR0 | Methane, bromonitro- | Nitrobromomethane | Bromonitromethane | bromo-nitromethane | Bromo-nitro-methane | CCRIS 9456 | monobromonitromethane | bromo(nitro)methane | UNII-EG63P9EUR0 | α-Bromonitromethane | CHEMBL2335229 |
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Why this grade ≥90% 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 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Overview Bromonitromethane has been used:
· in production of various protected α-bromo nitroalkane donors (including Fmoc) for use in Umpolung amide synthesis
· in preparation of (Z)-1-bromo-1-nitroalkenes via sodium iodide-catalyzed Henry reaction
· in diastereo- and enantioselective cyclopropanation of β,γ-unsaturated a-ketoesters via domino Michael-addition/intramolecular-alkylation strategy
Specifications Synonyms
1-bromonitromethane | EG63P9EUR0 | Methane, bromonitro- | Nitrobromomethane | Bromonitromethane | bromo-nitromethane | Bromo-nitro-methane | CCRIS 9456 | monobromonitromethane | bromo(nitro)methane | UNII-EG63P9EUR0 | α-Bromonitromethane | CHEMBL2335229 |
Specifications & Purity
≥90%
Names and Identifiers Canonical Smiles C([N+](=O)[O-])Br IUPAC Name bromo(nitro)methane InChIKey DNPRVXJGNANVCZ-UHFFFAOYSA-N INCHI 1S/CH2BrNO2/c2-1-3(4)5/h1H2 Isomeric SMILES C([N+](=O)[O-])Br WGK Germany 3 RTECS PA5360000 UN Number 3139 Molecular Weight 139.94 Reaxy-Rn 1741540 Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1741540&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 Organic 1,3-dipolar compounds Class Allyl-type 1,3-dipolar organic compounds Subclass Organic nitro compounds Intermediate Tree Nodes Not available Direct Parent C-nitro compounds Alternative Parents Propargyl-type 1,3-dipolar organic compounds Organic oxoazanium compounds Organopnictogen compounds Organonitrogen compounds Organobromides Organic oxides Hydrocarbon derivatives Alkyl bromides Molecular Framework Aliphatic acyclic compounds Substituents C-nitro compound - Propargyl-type 1,3-dipolar organic compound - Organic oxoazanium - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organonitrogen compound - Organobromide - Organohalogen compound - Alkyl halide - Alkyl bromide - Aliphatic acyclic compound Description This compound belongs to the class of organic compounds known as c-nitro compounds. These are compounds having the nitro group, -NO2 (free valence on nitrogen), which is attached to carbon. 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.
3D Structure Associated Targets(Human) Associated Targets(non-human) Mechanisms of Action Certificates（CoA,COO,BSE/TSE and Analysis Chart) Chemical and Physical Properties Refractive Index 1.496 Flash Point(°F) 235.4 °F Flash Point(°C) 113 °C Boil Point(°C) 146-148°C Molecular Weight 139.940 g/mol XLogP3 0.900 Hydrogen Bond Donor Count 0 Hydrogen Bond Acceptor Count 2 Rotatable Bond Count 0 Exact Mass 138.927 Da Monoisotopic Mass 138.927 Da Topological Polar Surface Area 45.800 Ų Heavy Atom Count 5 Formal Charge 0 Complexity 39.400 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
Citations of This Product References 1. Qian-Yuan Wu, Lu-Lin Yang, Xin-Yang Zhang, Wen-Long Wang, Yao Lu, Ye Du, Yun Lu, Hong-Ying Hu. (2020) Ammonia-Mediated Bromate Inhibition during Ozonation Promotes the Toxicity Due to Organic Byproduct Transformation. ENVIRONMENTAL SCIENCE & TECHNOLOGY, [PMID:32598842 ] [10.1021/acs.est.0c02984 ]
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