Description
2-Amino-3-(trifluoromethyl)pyridine (CAS No. 183610-70-0) is a high-purity fluorinated pyridine derivative widely utilized in pharmaceutical research, agrochemical development, and advanced material synthesis. With the molecular formula C6H5F3N2, this compound features a reactive amino group adjacent to an electron-withdrawing trifluoromethyl substituent, making it a versatile intermediate for nucleophilic substitution, cross-coupling reactions, and heterocyclic scaffold construction. Our product is rigorously tested to ensure ≥97% purity (GC/HPLC) and is supplied as a crystalline solid with excellent shelf stability under recommended storage conditions (2-8°C, inert atmosphere). Ideal for medicinal chemistry applications requiring trifluoromethylated building blocks, this compound is available in research (100g) quantities with customizable packaging options including amber glass vials and moisture-resistant containers.
Properties
- CAS Number: 183610-70-0
- Complexity: 134
- IUPAC Name: 3-(trifluoromethyl)pyridin-2-amine
- InChI: InChI=1S/C6H5F3N2/c7-6(8,9)4-2-1-3-11-5(4)10/h1-3H,(H2,10,11)
- InChI Key: YWOWJQMFMXHLQD-UHFFFAOYSA-N
- Exact Mass: 162.04048265
- Molecular Formula: C6H5F3N2
- Molecular Weight: 162.11
- SMILES: C1=CC(=C(N=C1)N)C(F)(F)F
- Topological: 38.9
- Monoisotopic Mass: 162.04048265
- Synonyms: 2-Amino-3-(trifluoromethyl)pyridine, 183610-70-0, DTXSID10375413, DTXCID30326442, 663-228-5, 3-(trifluoromethyl)pyridin-2-amine, 2-amino-3-trifluoromethylpyridine, 2-Pyridinamine, 3-(trifluoromethyl)-, 3-(Trifluoromethyl)-2-pyridinamine, MFCD04972538, 3-trifluoromethyl-pyridin-2-ylamine, EN300-117174, 3-(trifluoromethyl)-2-pyridylamine, SCHEMBL182868, SCHEMBL183159, SCHEMBL2067154, 2-amino-trifluoromethyl pyridine, SCHEMBL16445619, BDBM625990, RB1078, SBB051909, AKOS005064111, AB21173, AC-2718, CS-W010864, DS-0639, FS-1722, SY002651, 2-Amino-3-(trifluoromethyl)pyridine, 97%, DB-025287, DB-329855, ST50949493
2-Amino-3-(trifluoromethyl)pyridine serves as a key intermediate in the synthesis of trifluoromethyl-substituted pharmaceuticals, particularly kinase inhibitors and antiviral agents. The compound’s unique electronic properties facilitate its use in palladium-catalyzed cross-coupling reactions for constructing complex heterocycles. Researchers employ this building block to develop agrochemicals with enhanced metabolic stability due to the trifluoromethyl group’s lipophilicity. It also finds application in material science as a precursor for fluorinated liquid crystals and conductive polymers.
Safety and Hazards
GHS Hazard Statements
- H301 (97.5%): Toxic if swallowed [Danger Acute toxicity, oral]
- H317 (97.5%): May cause an allergic skin reaction [Warning Sensitization, Skin]
- H319 (100%): Causes serious eye irritation [Warning Serious eye damage/eye irritation]
Precautionary Statements
- P261, P264, P264+P265, P270, P272, P280, P301+P316, P302+P352, P305+P351+P338, P321, P330, P333+P317, P337+P317, P362+P364, P405, and P501
Hazard Classes and Categories
- Acute Tox. 3 (97.5%)
- Skin Sens. 1 (97.5%)
- Eye Irrit. 2A (100%)
If you are interested or have any questions, please contact us at support@atomfair.com
Disclaimer: Sold exclusively for laboratory research. Prohibited for commercial use, diagnostics, or human/animal applications. Buyers assume all compliance liability.


Reviews
There are no reviews yet.