Nom du produit:5-Thien-2-yl-7-(trifluoromethyl)[1,3]thiazolo[4,5-b]pyridin-2-amine

IUPAC Name:5-(thiophen-2-yl)-7-(trifluoromethyl)-[1,3]thiazolo[4,5-b]pyridin-2-amine

CAS:743453-27-2
Formule moléculaire:C11H6F3N3S2
Pureté:95%
Numéro de catalogue:CM366648
Poids moléculaire:301.31

Unité d'emballage Stock disponible Prix($) Quantité
CM366648-1g 3-4 Weeks ijħǎ

Pour une utilisation en R&D uniquement..

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Détails du produit

N° CAS:743453-27-2
Formule moléculaire:C11H6F3N3S2
Point de fusion:-
Code SMILES:NC1=NC2=NC(=CC(=C2S1)C(F)(F)F)C1=CC=CS1
Densité:
Numéro de catalogue:CM366648
Poids moléculaire:301.31
Point d'ébullition:
N° Mdl:MFCD05263794
Stockage:

Category Infos

Thiophenes
Thiophene is a five-membered heterocyclic compound containing a sulfur heteroatom with the molecular formula C4H4S. Thiophene is aromatic and is very similar to benzene; electrophilic substitution reaction is easier than benzene, and it is mainly substituted at the 2-position. Thiophene ring system has certain stability to oxidant.
Pyridines
Pyridine is a six-membered heterocyclic compound containing one nitrogen heteroatom. Pyridine and piperidine are the most frequently occurring heterocyclic building blocks in drug molecules. According to incomplete statistics, there are currently more than 180 drugs containing pyridine or piperidine structure that have been marketed, nearly 1/5 of the drugs approved for marketing in recent years contain these two structures.
Pyridine | C5H5N | Pyridine Supplier/Distributor/Manufacturer - Chemenu
Pyridine,Pyridine Wholesale,Pyridine for Sale,Pyridine Supplier,Pyridine Distributor,Pyridine Manufacturer
Pyridine is a basic heterocyclic organic compound with the chemical formula C5H5N. It is structurally related to benzene, with one methine group (=CH−) replaced by a nitrogen atom. It is a highly flammable, weakly alkaline, water-miscible liquid with a distinctive, unpleasant fish-like smell.
Thiazolopyridines
Thiazolopyridines are a class of heterocyclic compounds. Thiazolopyridines were developed as allosteric inhibitors of MALT1 with good cellular potency and refined selectivity.

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