5579-43-1 Usage
Uses
Used in Medicinal Chemistry:
5'',6'',7'',8''-TETRAHYDRO-3''H-SPIRO[CYCLOHEXANE-1,4''-QUINAZOLINE]-2''-THIOL is used as a key intermediate in the synthesis of various pharmaceutical compounds for its unique spirocyclic structure and thiol functional group.
Used in Drug Development:
In the pharmaceutical industry, 5'',6'',7'',8''-TETRAHYDRO-3''H-SPIRO[CYCLOHEXANE-1,4''-QUINAZOLINE]-2''-THIOL is used as a potential therapeutic agent for its potential biological and pharmacological properties, warranting further investigation into its properties and applications.
Used in Chemical Synthesis:
5'',6'',7'',8''-TETRAHYDRO-3''H-SPIRO[CYCLOHEXANE-1,4''-QUINAZOLINE]-2''-THIOL is used as a versatile building block in the synthesis of novel compounds with potential applications in various fields, including materials science and chemical research.
Further investigation into the properties and potential uses of 5'',6'',7'',8''-Tetrahydro-3''H-spiro[cyclohexane-1,4''-quinazoline]-2''-thiol could contribute to the development of new drugs and therapeutic agents, making it a valuable compound for ongoing research and development efforts.
Check Digit Verification of cas no
The CAS Registry Mumber 5579-43-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,5,7 and 9 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5579-43:
(6*5)+(5*5)+(4*7)+(3*9)+(2*4)+(1*3)=121
121 % 10 = 1
So 5579-43-1 is a valid CAS Registry Number.
5579-43-1Relevant academic research and scientific papers
Highly chemoselective multicomponent biginelli-type condensations of cycloalkanones, urea or thiourea and aldehydes
Zhu, Yu-Lin,Huang, Shen-Lin,Pan, Yuan-Jiang
, p. 2354 - 2367 (2007/10/03)
The classical Biginelli reaction is considerably extended by use of cycloalkanones instead of 1,3-dicarbonyl compounds. Use of TMSCl as a Lewis acid allowed one-pot chemoselective multicomponent Biginelli reactions between cycloalkanones, urea or thiourea, and aldehydes. Under similar reaction conditions, thiourea exhibited different behavior to urea, and aliphatic aldehydes showed lower reactivity than aromatic aldehydes. A possible mechanism to account for the reaction is proposed. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2005.
