67355-26-4 Usage
Uses
Used in Pharmaceutical Industry:
1,3-Thiazole-2,4-diamine hydrochloride is used as a reactant for the preparation of various thiazoles, which are important in the synthesis of pharmaceutical compounds. These thiazoles have been found to possess a range of biological activities, including antifungal, antibacterial, and antiviral properties, making them valuable in the development of new drugs.
Used in Chemical Synthesis:
In the chemical industry, 1,3-thiazole-2,4-diamine hydrochloride is utilized as a building block for the synthesis of more complex thiazole-containing molecules. These molecules can be further modified to enhance their reactivity and properties, leading to the development of new materials and compounds with potential applications in various fields.
Used in Reactive Modifications:
1,3-Thiazole-2,4-diamine hydrochloride is also used in the reactive modification of thiazole moieties. By altering the structure of the thiazole ring, chemists can create new compounds with improved properties or novel functions. This can be particularly useful in the development of new drugs, materials, or other chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 67355-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,3,5 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67355-26:
(7*6)+(6*7)+(5*3)+(4*5)+(3*5)+(2*2)+(1*6)=144
144 % 10 = 4
So 67355-26-4 is a valid CAS Registry Number.
67355-26-4Relevant articles and documents
Optimization of the manufacturing route to PF-610355 (1): Synthesis of intermediate 5
Content, Stephane,Dupont, Thomas,Fedou, Nicolas M.,Smith, Julian D.,Twiddle, Steven J. R.
, p. 193 - 201 (2013/05/08)
Tertiary carbinamine 5 is an isolated intermediate in the synthesis of a novel, inhaled β-2 adrenoreceptor agonist PF-610355. Process development for the key amide-formation and Ritter reactions, together with reaction understanding studies are discussed in context of the synthesis of 5. The optimized process employed to manufacture 140 kg of 5 is described, and was shown to have superior metrics to the preliminary commercial route.
