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1-Amino-6-(trifluoromethyl)-2,3-dihydro-1H-indene-1-carboxylic acid

CAS 1270535-90-4Formula C11H10F3NO2MW 245.2PubChem 124219938

1-Amino-6-(trifluoromethyl)-2,3-dihydro-1H-indene-1-carboxylic acid is a trifluoromethylated indane derivative featuring both amino and carboxylic acid functionalities. It serves as a versatile building block in organic synthesis, particularly for creating complex molecules with enhanced physicochemical properties for research applications.

Loading RDKit molecule structure...
InChIKey: ZJHMKOWBKOIGNN-UHFFFAOYSA-NC11H10F3NO2 | MW 245.2

Chemical Identity

Molecular Formula

C11H10F3NO2

Molecular Weight

245.2 g/mol

Exact Mass

245.066363

PubChem CID

124219938

IUPAC Name

1-amino-6-(trifluoromethyl)-2,3-dihydroindene-1-carboxylic acid

SMILES String

NC1(C(=O)O)CCc2ccc(C(F)(F)F)cc21

Names & Synonyms

1-Amino-6-(trifluoromethyl)indane-1-carboxylic acid1-AMINO-6-(TRIFLUOROMETHYL)-2,3-DIHYDRO-1H-INDENE-1-CARBOXYLICACID
External Identifiers
MFCD18678137

Catalog Overview

This compound, 1-Amino-6-(trifluoromethyl)-2,3-dihydro-1H-indene-1-carboxylic acid, is a chiral indane derivative incorporating a trifluoromethyl group at the 6-position and an amino and carboxylic acid group at the 1-position. The trifluoromethyl group is known to impart increased lipophilicity, metabolic stability, and modulate electronic properties, making it valuable in medicinal chemistry and agrochemical research. The amino and carboxylic acid functionalities provide reactive sites for various synthetic transformations, including amide bond formation, esterification, and salt formation, enabling its use in the construction...

Use Context

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

This compound, 1-Amino-6-(trifluoromethyl)-2,3-dihydro-1H-indene-1-carboxylic acid, is a chiral indane derivative incorporating a trifluoromethyl group at the 6-position and an amino and carboxylic acid group at the 1-position. The trifluoromethyl group is known to impart increased lipophilicity, metabolic stability, and modulate electronic properties, making it valuable in medicinal chemistry and agrochemical research. The amino and carboxylic acid functionalities provide reactive sites for various synthetic transformations, including amide bond formation, esterification, and salt formation, enabling its use in the construction of diverse chemical scaffolds.

Physical Data

Estimated

Estimated / predicted physical property values for catalog reference.

Appearance

White to off-white powder

Physical State

Solid

Melting Point

205.0 °C

Boiling Point

380.0 °C

Density

1.4 g/cm³

Water Solubility

Slightly soluble

Flash Point

250.0 °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 to avoid inhalation. Avoid contact with skin and eyes. In case of contact, rinse immediately with plenty of water. Always follow standard laboratory safety procedures and consult the Safety Data Sheet (SDS) for detailed handling and storage information. For research use only.

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: 292249GHS 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.