2-Bromopyridine - ≥98% , CAS No.109-04-6

CAS: 109-04-6 Cat. No.: B109679 Summenformel: C5H4BrN Molekulargewicht: 158 Beilstein Registry Number: 105789 EG-Nummer: 203-641-6
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GRADE & PURITY ≥98%
Synonyms
7Z7MLC4VD8 | Pyridine, bromo- | S12408 | 2-bromopridine | AM20050660 | B0650 | NSC 8031 | Pyridine, 2-bromo-, | a-Bromopyridine | FT-0611611 | NSC8031 | NSC-8031 | o-Bromopyridine | 2-bromanylpyridine | CHEBI:51574 | SCHEMBL6536 | 2 -bromopyridine | PS-42
Storage
Room temperature
Shipped In
Normal
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Size
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Qty
25g
B109679-25g
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22,47€

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Speichern 6,07 € (21.28%)
100g
B109679-100g
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4 Auf Lager

50,24€

62,39€
Speichern 12,15 € (19.47%)
250g
B109679-250g
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1 Auf Lager

103,17€

140,49€
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500g
B109679-500g
Auf Bestellung · 8–12 Wochen

157,84€

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Speichern 94,58 € (37.47%)
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Why this grade

≥98% 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.

Übersicht

2-Bromopyridine is a 2-halogenated pyridine used in the preparation of a variety of biologically active compounds such as antimalarial agents and beta-adrenoceptor agonist.
A pyridine used in the preparation of biologically active compounds

Specifications

Synonyme
7Z7MLC4VD8 | Pyridine, bromo- | S12408 | 2-bromopridine | AM20050660 | B0650 | NSC 8031 | Pyridine, 2-bromo-, | a-Bromopyridine | FT-0611611 | NSC8031 | NSC-8031 | o-Bromopyridine | 2-bromanylpyridine | CHEBI:51574 | SCHEMBL6536 | 2 -bromopyridine | PS-42
Spezifikationen & Reinheit
≥98%
Storage
Room temperature
Verschickt in
Normal
Reinheit
≥98%
Namen und Kennungen
Pubchem Sid488180632
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488180632
Kanonisches LächelnC1=CC=NC(=C1)Br
IUPAC Name2-bromopyridine
InChIKeyIMRWILPUOVGIMU-UHFFFAOYSA-N
INCHI1S/C5H4BrN/c6-5-3-1-2-4-7-5/h1-4H
Isomere SMILES C1=CC=NC(=C1)Br
WGK Deutschland 3
RTECS US3850000
UN-Nummer 2810
Verpackungsgruppe II
Molekulargewicht 158
Beilstein 105789
Reaxy-Rn 105789
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=105789&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

Taxonomy Tree

KingdomOrganic compounds
SuperclassOrganoheterocyclic compounds
KlassePyridines and derivatives
SubclassHalopyridines
Intermediate Tree Nodes Not available
Direct Parent2-halopyridines
Alternative Parents Aryl bromides  Heteroaromatic compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organobromides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents 2-halopyridine - Aryl halide - Aryl bromide - Heteroaromatic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Hydrocarbon derivative - Organonitrogen compound - Organobromide - Organohalogen compound - Aromatic heteromonocyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as 2-halopyridines. These are organic compounds containing a pyridine ring substituted at the 2-position by a halogen atom.
External Descriptors monobromopyridine
3D-Struktur
Interaktives chemisches Strukturmodell





Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

15 results found

Lot NumberCertificate TypeDatumArtikel
C2310729Certificate of AnalysisSep 03, 2026 B109679
B2219347Certificate of AnalysisAug 07, 2025 B109679
I2311219Certificate of AnalysisJun 11, 2025 B109679
I2311224Certificate of AnalysisJun 11, 2025 B109679
I2311269Certificate of AnalysisJun 11, 2025 B109679
E2324524Certificate of AnalysisApr 18, 2025 B109679
E2324514Certificate of AnalysisFeb 07, 2025 B109679
E2324516Certificate of AnalysisFeb 07, 2025 B109679
E2324526Certificate of AnalysisFeb 07, 2025 B109679
E2324528Certificate of AnalysisFeb 07, 2025 B109679
E2324538Certificate of AnalysisFeb 07, 2025 B109679
H2124079Certificate of AnalysisFeb 07, 2025 B109679
H2124080Certificate of AnalysisFeb 07, 2025 B109679
H2124081Certificate of AnalysisFeb 07, 2025 B109679
F2425101Certificate of AnalysisApr 01, 2024 B109679

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Chemische und physikalische Eigenschaften
LöslichkeitSoluble in water
Empfindlichkeitlight and heat and moisture sensitive
Brechungsindex 1.5705-1.5725
Flammpunkt (°F)54 °C
Flammpunkt (°C)54°C
Siedepunkt (°C)192-194°C
Molekulargewicht158.000 g/mol
XLogP31.400
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count1
Rotatable Bond Count0
Exact Mass156.953 Da
Monoisotopic Mass156.953 Da
Topological Polar Surface Area12.900 Ų
Heavy Atom Count7
Formal Charge0
Complexity56.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
FAQs und Artikel
From Piperidine to Pyridine: The “Most Common N-Heterocycle” Shift in FDA Small-Molecule New Drugs (2013–2023) and a Selection Guide (Tables 1–4)
A Practical Guide to Organozinc Reagents for Synthesis (Organozinc Reagents): Structural Features, Key Reactions, and a Practical Selection Navigation (Including Aladdin Product Tables)
Pyridine Research Selection Roadmap: Structural Features, Reaction Logic, and a Classification Navigator for Reagents/Building Blocks/Reference Standards (Tables 1–6)
Haloheterocycles and Cross-Coupling: A Research-Oriented Selection Framework from Substrate Identification to Bond-Forming Routes (Including Product Navigation and Tables 1–5)
Organic Brominated Heterocyclic Compounds: Structural Logic, Application Value, and Research Selection Guide (Tables 1–6)
From Nitroarenes to Pharmaceutically Relevant Pyridines: A Photochemically Induced Aryl Nitrene-Mediated Skeletal Editing Strategy
One-Pot Arylation of the Piperidine α-C–H Bond: From Directed Lithiation and Li→Zn Transmetalation to Negishi Coupling
Citations of This Product
Referenzen
1. Lihua Ma, Song Guo, Jifu Sun, Caishun Zhang, Jianzhang Zhao, Huimin Guo.  (2013)  Green light-excitable naphthalenediimide acetylide-containing cyclometalated Ir(III) complex with long-lived triplet excited states as triplet photosensitizers for triplet–triplet annihilation upconversion.  DALTON TRANSACTIONS,  42  (18): (6478-6488).  [PMID:23471114] [10.1039/C3DT32815E]
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