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5-Bromo-2-hydroxy-6-methyl-4-(trifluoromethyl)nicotinonitrile

CAS 1092352-76-5Formula C8H4BrF3N2OMW 281.03PubChem 30772179

5-Bromo-2-hydroxy-6-methyl-4-(trifluoromethyl)nicotinonitrile is a halogenated nicotinonitrile derivative, often utilized in synthetic organic chemistry as a versatile building block for the creation of more complex chemical structures, particularly within drug discovery and agrochemical research.

Loading RDKit molecule structure...
InChIKey: LDROYAOVNZFOPG-UHFFFAOYSA-NC8H4BrF3N2O | MW 281.03

Chemical Identity

Molecular Formula

C8H4BrF3N2O

Molecular Weight

281.03 g/mol

Exact Mass

279.94591

PubChem CID

30772179

IUPAC Name

5-bromo-6-methyl-2-oxo-4-(trifluoromethyl)-1H-pyridine-3-carbonitrile

SMILES String

Cc1nc(O)c(C#N)c(C(F)(F)F)c1Br

Names & Synonyms

5-Bromo-2-hydroxy-6-methyl-4-(trifluoromethyl)-nicotinonitrile5-bromo-2-hydroxy-6-methyl-4-(trifluoromethyl)pyridine-3-carbonitrileAS-813/435019025-Bromo-1,2-dihydro-6-methyl-2-oxo-4-(trifluoromethyl)-3-pyridinecarbonitrile
External Identifiers
MFCD11501053AKOS005073115KC-0712DB-397991CS-0367162

Catalog Overview

5-Bromo-2-hydroxy-6-methyl-4-(trifluoromethyl)nicotinonitrile is an organic compound characterized by a pyridine core substituted with a bromine atom, a hydroxyl group, a methyl group, a trifluoromethyl group, and a nitrile group. Its molecular formula is C8H4BrF3N2O and its molecular weight is approximately 281. 03 g/mol. This compound's diverse functional groups make it a valuable intermediate in the synthesis of various heterocyclic compounds and potential bioactive molecules.

Use Context

  • Research chemical sourcing
  • Custom synthesis and catalog availability review
  • COA, SDS, pricing, and fulfillment workflow
Read more catalog context

5-Bromo-2-hydroxy-6-methyl-4-(trifluoromethyl)nicotinonitrile is an organic compound characterized by a pyridine core substituted with a bromine atom, a hydroxyl group, a methyl group, a trifluoromethyl group, and a nitrile group. Its molecular formula is C8H4BrF3N2O and its molecular weight is approximately 281.03 g/mol. This compound's diverse functional groups make it a valuable intermediate in the synthesis of various heterocyclic compounds and potential bioactive molecules. It is classified as a research-oriented/research-oriented compound, suggesting its relevance in medicinal chemistry and related fields for developing novel chemical entities.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White solid

Physical State

Solid

Melting Point

180.0 °C

Boiling Point

350.0 °C

Density

1.7 g/cm³

Water Solubility

Slightly soluble

Flash Point

185.0 °C

Applications / Classifications

Research intermediateCustom synthesis building block

Biological Target Reference

No verified biological target assignment. This compound is listed primarily as a research or synthetic intermediate.

Preliminary Safety-Style Reference

Preliminary

Preliminary safety-style information for reference only. Not a supplier SDS.

Handling and Storage
  • Handle 5-Bromo-2-hydroxy-6-methyl-4-(trifluoromethyl)nicotinonitrile with appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Use in a well-ventilated area or under a fume hood to avoid inhalation. Avoid contact with skin and eyes. In case of contact, rinse immediately with plenty of water. Store in a cool, dry place, away from incompatible materials. Always consult the Safety Data Sheet (SDS) for detailed hazard information and safe handling procedures before use.

Related Products / Graph Discovery

Related products, derivatives, keywords, and application cues for catalog discovery.

Similar products (text references)

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Recommended application cues

Research intermediateCustom synthesis building block

Catalog discovery cues, not supplier-verified claims.

Related HS Code / Compliance

HS Code: 293339GHS Pictograms: GHS07Shipment review: Shipment details require review before fulfillment.

Compliance cues are non-linked reference tags and require shipment review.

Catalog navigation

Other public CAS pages in this catalog. These links support navigation across additional intermediates and do not imply equivalence, availability, or shared use.