153471-67-1 Usage
Uses
Used in Chemical Synthesis:
(2-Chlorothiazol-5-yl)methylamine Hydrochloride is used as a chemical intermediate for the synthesis of various organic compounds and pharmaceuticals. Its unique structure allows it to be a versatile building block in the creation of complex molecules.
Used in Pharmaceutical Industry:
(2-Chlorothiazol-5-yl)methylamine Hydrochloride is used as a key component in the development of new drugs, particularly in the area of medicinal chemistry. Its reactivity and structural features make it a valuable asset in the design and synthesis of potential therapeutic agents.
Used in Research and Development:
(2-Chlorothiazol-5-yl)methylamine Hydrochloride is used as a research compound for studying the properties and reactions of organothiazoles. It can provide insights into the behavior of similar compounds and contribute to the advancement of chemical knowledge in this area.
Check Digit Verification of cas no
The CAS Registry Mumber 153471-67-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,3,4,7 and 1 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 153471-67:
(8*1)+(7*5)+(6*3)+(5*4)+(4*7)+(3*1)+(2*6)+(1*7)=131
131 % 10 = 1
So 153471-67-1 is a valid CAS Registry Number.
InChI:InChI=1/C4H5ClN2S.ClH/c1-6-3-2-7-4(5)8-3;/h2,6H,1H3;1H
153471-67-1Relevant academic research and scientific papers
PROCESS FOR PRODUCING AN AMINOMETHYL THIAZOLE COMPOUND
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Page/Page column 15-17, (2008/06/13)
A process for producing a thiazole compound of the formula (3): wherein X1 is a hydrogen atom or a halogen atom, which comprises reacting a compound of the formula (1): wherein X1 is as defined above, and X2 represents a halogen atom, with ammonia and formaldehyde to obtain a hexahydrotriazine compound of the formula (2): wherein X1 is as defined above, and reacting the resulting hexahydrotriazine compound with hydroxylamine under acidic conditions. According to this process, the thiazole compound of the formula (3) can be industrially advantageously produced using inexpensive ammonia with suppressing the formation of a byproduct of the formula (4): wherein X1 is as defined above.
