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3H-Spiro[1,3-benzothiazole-2,1'-cyclohexane] is a heterocyclic chemical compound characterized by its unique spirocyclic structure, which incorporates both a benzothiazole and cyclohexane moiety. 3H-Spiro[1,3-benzothiazole-2,1'-cyclohexane] holds potential biological activity and is of interest in the field of medicinal chemistry due to its possible interactions with biological targets, making it a candidate for pharmaceutical applications and drug development.

182-53-6

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182-53-6 Usage

Uses

Used in Pharmaceutical Applications:
3H-Spiro[1,3-benzothiazole-2,1'-cyclohexane] is used as a potential therapeutic agent for its ability to engage with biological targets, which may lead to the development of new drugs or the enhancement of existing ones. Its unique structure is under investigation for its contribution to pharmacological properties, which could be harnessed for treating various medical conditions.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 3H-Spiro[1,3-benzothiazole-2,1'-cyclohexane] serves as a subject of study to explore its potential as a lead compound in drug development. 3H-Spiro[1,3-benzothiazole-2,1'-cyclohexane]'s interaction with biological systems is being researched to understand its full potential and to identify any therapeutic applications it may possess.
Further research is essential to comprehensively evaluate the properties and possible applications of 3H-Spiro[1,3-benzothiazole-2,1'-cyclohexane], ensuring its safety and efficacy in any potential pharmaceutical use.

Check Digit Verification of cas no

The CAS Registry Mumber 182-53-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,8 and 2 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 182-53:
(5*1)+(4*8)+(3*2)+(2*5)+(1*3)=56
56 % 10 = 6
So 182-53-6 is a valid CAS Registry Number.

182-53-6Relevant articles and documents

BORANE-TETRAHYDROFURAN AS A USEFUL REAGENT IN THE N-MONOALKYLATION OF AMINES AND AMINOALCOHOLS BY CARBONYL COMPOUNDS.

Morales, Hilda R.,Perez-Juarez, Martin,Cuellar, Laura,Mendoza, Lourdes,Fernandez, Hector,Contreras, Rosalinda

, p. 1213 - 1220 (2007/10/02)

A new procedure for the high-yield N-monoalkylation of primary aromatic and aliphatic amines is described.

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