2-Amino-5-Cbz-4,5,6,7-tetrahydro-1,3-thiazolo[5,4-c]pyridine(CAS#1141669-69-3)

Introduction

2-Amino-5-CBZ-4,5,6,7-tetrahydrothiazol[5,4-C]pyridine is an organic compound. The following is an introduction to the properties, uses, preparation methods and safety information of this compound:Quality:- Appearance: 2-Amino-5-CBZ-4,5,6,7-tetrahydrothiazol[5,4-C]pyridine is a white to light yellow crystalline solid.- Solubility: Soluble in most organic solvents such as methanol, dimethylformamide and methylene chloride.- Stability: This compound is sensitive to light, heat, and humidity and should be stored in a cool, dry place.Use:2-Amino-5-CBZ-4,5,6,7-tetrahydrothiazolo[5,4-C]pyridine is an important intermediate compound with a wide range of uses, including:- Chemical research: as a substrate or reagent for organic synthesis reactions, it has high reactivity.Method:The preparation methods of 2-amino-5-CBZ-4,5,6,7-tetrahydrothiazolo[5,4-C]pyridine are generally complex, and the commonly used synthetic routes include multi-step reactions such as thiazole ring formation, ring modification and amination.Safety Information:- The safety of 2-amino-5-CBZ-4,5,6,7-tetrahydrothiazolo[5,4-C]pyridine has not been fully studied and evaluated, and its use should be based on laboratory safety practices.- Personal protective equipment such as protective gloves, goggles, and masks should be worn when handling and using compounds to avoid contact with skin, eyes, and inhalation.- Waste disposal: Waste should be sorted and disposed of in accordance with local laws and regulations to avoid environmental pollution.

Application

2‑Amino‑5‑Cbz‑4,5,6,7‑tetrahydro‑1,3‑thiazolo[5,4‑c]pyridine (CAS 1141669‑69‑3) is a Cbz‑protected bicyclic heterocycle widely utilized in medicinal chemistry as a versatile building block to construct drug‑like libraries for drug discovery. The fused thiazole‑pyridine core serves as a key intermediate for the development of potent kinase inhibitors (e.g., MALT1, c‑KIT, Bcr‑Abl) targeting oncology, autoimmune diseases, neurological disorders, and asthma. Its derivatives also demonstrate significant anticancer, anti‑inflammatory, antibacterial, and antiviral activities. The Cbz protecting group enables stepwise functionalization and selective deprotection for assembling complex pharmacophores. Xinchem offers custom synthesis and contract manufacturing of this high‑purity heterocyclic scaffold with flexible scaling from R&D to commercial tons. Contact us today for a competitive quote and reliable global supply.