Description

5-Bromo-2-ethoxypyridine (CAS No. 55849-30-4) is a high-purity organic compound with the molecular formula C₇H₈BrNO. This versatile pyridine derivative is widely used as a key intermediate in pharmaceutical synthesis, agrochemical production, and materials science research. Its unique bromo-ethoxy substitution pattern makes it particularly valuable for nucleophilic aromatic substitution reactions and metal-catalyzed cross-coupling reactions. Our product is supplied as a crystalline solid with ≥97% purity (GC), rigorously tested to meet the exacting standards of research and industrial applications. Suitable for use in medicinal chemistry, chemical biology, and as a building block for more complex heterocyclic systems.

Key Features:
– High chemical purity (≥97%)
– Excellent batch-to-batch consistency
– Optimal for Suzuki, Stille, and other palladium-catalyzed couplings
– Stable under standard storage conditions
– Available in various packaging options from milligrams to kilograms

Properties

• CAS Number: 55849-30-4
• Complexity: 99.6
• IUPAC Name: 5-bromo-2-ethoxy-pyridine
• InChI: InChI=1S/C7H8BrNO/c1-2-10-7-4-3-6(8)5-9-7/h3-5H,2H2,1H3
• InChI Key: WQXZKMUZWPUZGL-UHFFFAOYSA-N
• Exact Mass: 200.97893
• Molecular Formula: C7H8BrNO
• Molecular Weight: 202.05
• SMILES: CCOC1=NC=C(C=C1)Br
• Topological: 22.1
• Monoisotopic Mass: 200.97893
• Synonyms: 5-Bromo-2-ethoxypyridine, 55849-30-4, DTXSID50355774, DTXCID60306833, 611-323-7, 2-ethoxy-5-bromopyridine, 3-BROMO-6-ETHOXYPYRIDINE, MFCD00234311, Pyridine, 5-bromo-2-ethoxy-, 5-bromo-2-ethoxy-pyridine, 5-bromo-ethoxy-pyridine, SCHEMBL156935, 5-bromo-2-(ethyloxy)pyridine, SCHEMBL27868772, 5-Bromo-2-ethoxypyridine, 97%, WQXZKMUZWPUZGL-UHFFFAOYSA-N, SBB054264, AKOS005199250, AB05210, AC-5974, DS-0799, FS-1790, SY018882, DB-003987, B3673, CS-0014710, NS00126419, ST50826889, EN300-225185, AC-907/25004667

5-Bromo-2-ethoxypyridine serves as a crucial building block in medicinal chemistry for the synthesis of biologically active compounds. The bromine substituent enables facile cross-coupling reactions to create more complex pharmaceutical intermediates. Researchers utilize this compound in the development of kinase inhibitors and other therapeutic agents. Its ethoxy group provides both electronic modulation and potential metabolic stability in drug discovery programs.

Safety and Hazards

GHS Hazard Statements

• H302 (97.8%): Harmful if swallowed [Warning Acute toxicity, oral]
• H315 (97.8%): Causes skin irritation [Warning Skin corrosion/irritation]
• H317 (87%): May cause an allergic skin reaction [Warning Sensitization, Skin]
• H318 (95.7%): Causes serious eye damage [Danger Serious eye damage/eye irritation]
• H335 (95.7%): May cause respiratory irritation [Warning Specific target organ toxicity, single exposure; Respiratory tract irritation]

Precautionary Statements

• P261, P264, P264+P265, P270, P271, P272, P280, P301+P317, P302+P352, P304+P340, P305+P354+P338, P317, P319, P321, P330, P332+P317, P333+P317, P362+P364, P403+P233, P405, and P501

Hazard Classes and Categories

• Acute Tox. 4 (97.8%)
• Skin Irrit. 2 (97.8%)
• Skin Sens. 1 (87%)
• Eye Dam. 1 (95.7%)
• STOT SE 3 (95.7%)

If you are interested or have any questions, please contact us at support@atomfair.com

Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.