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5-(1-Methylcyclopropyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-2-carboxylic acid

CAS 436088-38-9Formula C12H10F3N3O2MW 285.22PubChem 3145956

5-(1-Methylcyclopropyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-2-carboxylic acid is a pyrazolopyrimidine derivative featuring a trifluoromethyl group and a carboxylic acid moiety, making it a valuable compound for research in medicinal chemistry and drug discovery.

Loading RDKit molecule structure...
InChIKey: UVQZUXPEYVUBAO-UHFFFAOYSA-NC12H10F3N3O2 | MW 285.22

Chemical Identity

Molecular Formula

C12H10F3N3O2

Molecular Weight

285.22 g/mol

Exact Mass

285.072511

PubChem CID

3145956

SMILES String

CC1(c2cc(C(F)(F)F)n3nc(C(=O)O)cc3n2)CC1

Names & Synonyms

5-(1-Methyl-cyclopropyl)-7-trifluoromethyl-pyrazolo[1,5-a]pyrimidine-2-carboxylic acidHMS2471O18BAS 03183145Pyrazolo[1,5-a]pyrimidine-2-carboxylicacid, 5-(1-methylcyclopropyl)-7-(trifluoromethyl)-
External Identifiers
SMR000124866MLS000067414CHEMBL1598221DTXSID80389820AKOS000557005SR-01000325102SR-01000325102-1

Catalog Overview

5-(1-Methylcyclopropyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-2-carboxylic acid, identified by CAS 436088-38-9, is an organic compound with the molecular formula C12H10F3N3O2 and a molecular weight of 285. 22 g/mol. This compound belongs to the pyrazolopyrimidine class, characterized by a fused bicyclic ring system. It incorporates a 1-methylcyclopropyl substituent at the 5-position, a trifluoromethyl group at the 7-position, and a carboxylic acid group at the 2-position.

Use Context

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

5-(1-Methylcyclopropyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-2-carboxylic acid, identified by CAS 436088-38-9, is an organic compound with the molecular formula C12H10F3N3O2 and a molecular weight of 285.22 g/mol. This compound belongs to the pyrazolopyrimidine class, characterized by a fused bicyclic ring system. It incorporates a 1-methylcyclopropyl substituent at the 5-position, a trifluoromethyl group at the 7-position, and a carboxylic acid group at the 2-position. Its 'druglike_bioactive_like' structural bucket suggests its potential utility as a scaffold or building block in the synthesis of novel chemical entities for pharmaceutical research and development.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White solid

Physical State

Solid

Melting Point

165.0 °C

Boiling Point

308.0 °C

Density

1.4 g/cm³

Water Solubility

Slightly soluble

Flash Point

220.0 °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-(1-Methylcyclopropyl)-7-(trifluoromethyl)pyrazolo[1,5-a]pyrimidine-2-carboxylic acid with appropriate personal protective equipment, including gloves, eye protection, and a lab coat. Use in a well-ventilated area or fume hood to avoid inhalation. Avoid contact with skin and eyes. In case of contact, rinse thoroughly with water. Store in a cool, dry place, away from incompatible materials. Always refer to the Safety Data Sheet (SDS) for comprehensive safety information before handling.

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: 293399GHS 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.