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tert-Butyl (3-chloro-6-fluoro-9H-pyrido[2,3-b]indol-8-yl)(methyl)carbamate

CAS 2245358-13-6Formula C17H17ClFN3O2MW 349.8PubChem 135347135

tert-Butyl (3-chloro-6-fluoro-9H-pyrido[2,3-b]indol-8-yl)(methyl)carbamate is a complex organic compound with the CAS number 2245358-13-6. Featuring a pyrido[2,3-b]indole core, it is primarily intended for research and development applications.

Loading RDKit molecule structure...
InChIKey: LHPGCRZPGPBWLL-UHFFFAOYSA-NC17H17ClFN3O2 | MW 349.8

Chemical Identity

Molecular Formula

C17H17ClFN3O2

Molecular Weight

349.8 g/mol

Exact Mass

349.099333

PubChem CID

135347135

IUPAC Name

tert-butyl N-(3-chloro-6-fluoro-9H-pyrido[2,3-b]indol-8-yl)-N-methylcarbamate

SMILES String

CN(C(=O)OC(C)(C)C)c1cc(F)cc2c1[nH]c1ncc(Cl)cc12

Names & Synonyms

TERT-BUTYL N-(3-CHLORO-6-FLUORO-9H-PYRIDO[2,3-B]INDOL-8-YL)-N-METHYL-CARBAMATEtert-butyl N-{3-chloro-6-fluoro-9H-pyrido[2,3-b]indol-8-yl}-N-methylcarbamateC17H17ClFN3O2
External Identifiers
SCHEMBL20522023SCHEMBL30152873AT26106CS-0130840

Catalog Overview

tert-Butyl (3-chloro-6-fluoro-9H-pyrido[2,3-b]indol-8-yl)(methyl)carbamate, identified by CAS 2245358-13-6, is a synthetic organic chemical with the molecular formula C17H17ClFN3O2 and a molecular weight of 349. 80. This compound incorporates a pyrido[2,3-b]indole heterocyclic system, substituted with chloro and fluoro groups, and a tert-butyl methylcarbamate moiety. Its intricate structure suggests potential utility as a building block in medicinal chemistry, drug discovery, or as a reference standard in analytical research.

Use Context

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

tert-Butyl (3-chloro-6-fluoro-9H-pyrido[2,3-b]indol-8-yl)(methyl)carbamate, identified by CAS 2245358-13-6, is a synthetic organic chemical with the molecular formula C17H17ClFN3O2 and a molecular weight of 349.80. This compound incorporates a pyrido[2,3-b]indole heterocyclic system, substituted with chloro and fluoro groups, and a tert-butyl methylcarbamate moiety. Its intricate structure suggests potential utility as a building block in medicinal chemistry, drug discovery, or as a reference standard in analytical research. It is classified within the 'druglike_bioactive_like' structural bucket, indicating its relevance in the synthesis of compounds with potential biological activity.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White crystalline powder

Physical State

Solid

Melting Point

175.0 °C

Boiling Point

450.0 °C

Density

1.4 g/cm³

Water Solubility

Insoluble

Flash Point

280.0 °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 with appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Use in a well-ventilated area or fume hood. Avoid inhalation, ingestion, and skin contact. Refer to the Safety Data Sheet (SDS) for detailed hazard information and safe handling procedures. Store in a cool, dry place, away from incompatible materials.

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: 29339990GHS 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.