1245914-66-2

Basic information

• Product Name: 1H-Pyrrolo[2,3-c]pyridine, 2,3-dihydro-5-(trifluoromethyl)-
• CAS NO: 1245914-66-2
• Mol File: 1245914-66-2.mol
• Article Data: 0

Chemical Properties

• CAS DataBase Reference: 1H-Pyrrolo[2,3-c]pyridine, 2,3-dihydro-5-(trifluoromethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Pyrrolo[2,3-c]pyridine, 2,3-dihydro-5-(trifluoromethyl)-(1245914-66-2)
• EPA Substance Registry System: 1H-Pyrrolo[2,3-c]pyridine, 2,3-dihydro-5-(trifluoromethyl)-(1245914-66-2)

Safety Data

• Hazardous Substances Data: 1245914-66-2(Hazardous Substances Data)

Usage

Pyrrolopyridine ring system

A ring structure consisting of a pyrrole ring fused to a pyridine ring This is the specific type of heterocyclic ring system present in the compound.

Trifluoromethyl group

A functional group consisting of a carbon atom bonded to three fluorine atoms (CF3) This group is attached to the compound and contributes to its properties.

Pharmaceutical industry use

Commonly used as a building block for the synthesis of various drug compounds This describes the primary application of the compound in the pharmaceutical field.

Unique structure and properties

The compound's specific arrangement of atoms and its properties make it valuable for the development of new pharmaceuticals with potential therapeutic applications This highlights the importance of the compound in creating new drugs.

High lipophilicity

The presence of the trifluoromethyl group increases the compound's affinity for lipids, which can impact its pharmacokinetic and pharmacodynamic properties This refers to how the compound's affinity for lipids can affect its absorption, distribution, metabolism, and excretion in the body, as well as its therapeutic effects.