2-Bromo-5-nitropyridine - ≥98% , CAS No.4487-59-6

CAS: 4487-59-6 Cat. No.: B107718 Peso molecular: 202.99 Beilstein Registry Number: 20(5)5,455 Número EC: 224-777-2
Disponible para pedir
GRADE & PURITY ≥98%
Synonyms
DTXSID10196327 | HUUFTVUBFFESEN-UHFFFAOYSA-N | Silanol, 1,4-phenylenebis[dimethyl- | FT-0611499 | BCP22145 | NSC 73702 | 2-Bromo-5-nitropyridine | 2-bromo-5-nitro-pyridine | A872458 | AC-9485 | MFCD00006222 | FG-0508 | Bis(2-aminoethyl) Ether | HY-W007858
Storage
Room temperature
Shipped In
Normal
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
1g
B107718-1g
5
9,90US$
5g
B107718-5g
5
10,90US$
10g
B107718-10g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
11,90US$
25g
B107718-25g
3

25,90US$

38,90US$
Guardar 13,00 US$ (33.42%)
100g
B107718-100g
4

97,90US$

146,90US$
Guardar 49,00 US$ (33.36%)
500g
B107718-500g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.

248,90US$

373,90US$
Guardar 125,00 US$ (33.43%)
Enter a quantity for the sizes you want to add.
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Why this grade

≥98% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Room temperature Ships Normal Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 1 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
DTXSID10196327 | HUUFTVUBFFESEN-UHFFFAOYSA-N | Silanol, 1, 4-phenylenebis[dimethyl- | FT-0611499 | BCP22145 | NSC 73702 | 2-Bromo-5-nitropyridine | 2-bromo-5-nitro-pyridine | A872458 | AC-9485 | MFCD00006222 | FG-0508 | Bis(2-aminoethyl) Ether | HY-W007858
Especificaciones y pureza
≥98%
Condiciones de almacenamiento de almacenamiento
Room temperature
Enviado en
Normal
Pureza
≥98%
Nombres e identificadores
Pubchem Sid488185543
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488185543
Sonrisas canónicasC1=CC(=NC=C1[N+](=O)[O-])Br
IUPAC Name2-bromo-5-nitropyridine
InChIKeyHUUFTVUBFFESEN-UHFFFAOYSA-N
INCHI1S/C5H3BrN2O2/c6-5-2-1-4(3-7-5)8(9)10/h1-3H
Isómeros SMILES C1=CC(=NC=C1[N+](=O)[O-])Br
WGK Alemania 3
Número ONU 2811
Peso molecular 202.99
Beilstein 20(5)5,455
Reaxy-Rn 120901
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=120901&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
SuperclassOrganic 1,3-dipolar compounds
ClaseAllyl-type 1,3-dipolar organic compounds
SubclassOrganic nitro compounds
Intermediate Tree Nodes C-nitro compounds
Direct ParentNitroaromatic compounds
Alternative Parents 2-halopyridines  Aryl bromides  Heteroaromatic compounds  Propargyl-type 1,3-dipolar organic compounds  Organic oxoazanium compounds  Azacyclic compounds  Organopnictogen compounds  Organonitrogen compounds  Organobromides  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAromatic heteromonocyclic compounds
Substituents Nitroaromatic compound - 2-halopyridine - Aryl bromide - Aryl halide - Pyridine - Heteroaromatic compound - Organic oxoazanium - Propargyl-type 1,3-dipolar organic compound - Organoheterocyclic compound - Azacycle - Organic nitrogen compound - Organopnictogen compound - Organonitrogen compound - Organobromide - Organic oxygen compound - Organohalogen compound - Organic oxide - Hydrocarbon derivative - Aromatic heteromonocyclic compound
DescripciónThis compound belongs to the class of organic compounds known as nitroaromatic compounds. These are c-nitro compounds where the nitro group is C-substituted with an aromatic group.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Certificados (CoA, COO, BSE/TSE y tabla de análisis)
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.

9 results found

Lot NumberCertificate TypeFechaArticulo
H2005107Certificate of AnalysisDec 22, 2025 B107718
E2203034Certificate of AnalysisNov 07, 2025 B107718
E2203035Certificate of AnalysisNov 07, 2025 B107718
E2203051Certificate of AnalysisNov 07, 2025 B107718
E2203058Certificate of AnalysisNov 07, 2025 B107718
H2525012Certificate of AnalysisSep 01, 2025 B107718
E2325124Certificate of AnalysisFeb 11, 2025 B107718
B1614020Certificate of AnalysisJun 05, 2023 B107718
C2310677Certificate of AnalysisMar 18, 2023 B107718
Propiedades químicas y físicas
SolubilidadInsoluble in water.
Punto de ebullición (°C)147 °C/10 mmHg
Punto de fusión (°C)139-141°C
Peso molecular202.990 g/mol
XLogP32.300
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count3
Rotatable Bond Count0
Exact Mass201.938 Da
Monoisotopic Mass201.938 Da
Topological Polar Surface Area58.700 Ų
Heavy Atom Count10
Formal Charge0
Complexity136.000
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
Citations of This Product
Referencias
1. Fu Fengping, He Qian, Zhao Shizheng, Zhu Ting, Liao Fang.  (2021)  Synthesis of photoluminescent m-phenylenediamine-Rhodamine B copolymer dots: selective ultrahigh photocatalytic performance for catalytic reduction of nitro-compound.  RESEARCH ON CHEMICAL INTERMEDIATES,  47  (10): (4173-4192).  [PMID:] [10.1007/s11164-021-04512-9]
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