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Tert-butyl 6-chloro-2-methylquinoline-4-carboxylate

CAS 1033194-62-5Formula C15H16ClNO2MW 277.74PubChem 45926101

Tert-butyl 6-chloro-2-methylquinoline-4-carboxylate is a quinoline derivative with a tert-butyl ester and a chlorine substituent, primarily used in chemical synthesis and medicinal chemistry research.

Loading RDKit molecule structure...
InChIKey: KFTZRUWMBAAWHA-UHFFFAOYSA-NC15H16ClNO2 | MW 277.74

Chemical Identity

Molecular Formula

C15H16ClNO2

Molecular Weight

277.74 g/mol

Exact Mass

277.086956

PubChem CID

45926101

SMILES String

Cc1cc(C(=O)OC(C)(C)C)c2cc(Cl)ccc2n1

Names & Synonyms

tert-Butyl6-chloro-2-methylquinoline-4-carboxylateAR3278F306474tert-butyl 6-chloro-2-methyl-quinoline-4-carboxylate1,1-Dimethylethyl 6-chloro-2-methyl-4-quinolinecarboxylate
External Identifiers
MFCD11040524DTXSID401192777AKOS027334977SB69410AS-45568CS-0172995

Catalog Overview

Tert-butyl 6-chloro-2-methylquinoline-4-carboxylate is an organic compound characterized by a quinoline core substituted with a methyl group at position 2, a chlorine atom at position 6, and a tert-butyl carboxylate group at position 4. With a molecular formula of C15H16ClNO2 and a molecular weight of 277.74 g/mol, this compound is a valuable building block in synthetic organic chemistry. Its structural features, including the heterocyclic quinoline ring and the ester functionality, make it suitable for various chemical transformations and for the synthesis of more complex molecules, particularly those with potential biological...

Use Context

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

Tert-butyl 6-chloro-2-methylquinoline-4-carboxylate is an organic compound characterized by a quinoline core substituted with a methyl group at position 2, a chlorine atom at position 6, and a tert-butyl carboxylate group at position 4. With a molecular formula of C15H16ClNO2 and a molecular weight of 277.74 g/mol, this compound is a valuable building block in synthetic organic chemistry. Its structural features, including the heterocyclic quinoline ring and the ester functionality, make it suitable for various chemical transformations and for the synthesis of more complex molecules, particularly those with potential biological activity. It is typically handled as a research-use-only chemical.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

white crystalline powder

Physical State

solid

Melting Point

145.0 °C

Boiling Point

405.0 °C

Density

1.22 g/cm³

Water Solubility

insoluble

Flash Point

199.6 °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
  • For research use only. Handle Tert-butyl 6-chloro-2-methylquinoline-4-carboxylate in a well-ventilated area or fume hood. Wear appropriate personal protective equipment, including safety glasses, gloves, and a lab coat, to prevent skin and eye contact. Avoid inhalation of dust or vapors. In case of contact, rinse thoroughly with water. Store in a cool, dry place, away from incompatible materials. Consult the Safety Data Sheet (SDS) for detailed hazard information and safe handling procedures.

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: 293349GHS 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.