80563-98-0 Usage
Spiro compound family
Yes
A spiro compound is characterized by a carbon atom connected to two non-adjacent atoms through single bonds, forming a spiro center.
Contains two sulfur atoms
Yes
The compound has two sulfur atoms in its structure, which contribute to its unique properties and reactivity.
Cyclic structure
Yes
The compound has a closed ring structure, which is a common feature in many organic compounds.
Used in organic synthesis
Yes
1,4-Dithiaspiro[4.5]decan-7-one is utilized as a building block or intermediate in the synthesis of various organic compounds.
Building block in pharmaceuticals and fine chemicals
Yes
Due to its unique structure and reactivity, the compound is used in the production of pharmaceuticals and fine chemicals.
Potential applications in materials science
Yes
The compound's properties may be exploited in the development of new materials with specific characteristics.
Potential applications in drug discovery
Yes
The compound's unique structure and reactivity make it a candidate for use in the development of new drugs and therapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 80563-98-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,6 and 3 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 80563-98:
(7*8)+(6*0)+(5*5)+(4*6)+(3*3)+(2*9)+(1*8)=140
140 % 10 = 0
So 80563-98-0 is a valid CAS Registry Number.
80563-98-0Relevant articles and documents
Ring-opening reactions of donor-acceptor cyclopropanes with cyclic ketals and thiol ketals
Cai, Hu,Chen, Yan,Cheng, Qihang,Yin, Lei,Zhang, Dongxin,Zhang, Qian-Feng,Zhong, Junchao
supporting information, p. 6492 - 6496 (2020/11/10)
1,3-Cyclohexandione derived cyclic ketals and thiol ketals were used as O- and S-nucleophiles, respectively, for the ring opening of donor-acceptor cyclopropanes catalyzed by Cu(OTf)2 and a series of functionalized alkylene glycol diethers and dithiol diethers were obtained in good to high yields under mild conditions. This journal is
The substrate- and stereoselectivity of microbial reductions of 1,4-dithiaspirodecanones and 1,5-dithiaspiroundecanones
Takemura, Tetsuo,Hosoya, Yoshiko,Mori, Nobuo
, p. 523 - 529 (2007/10/02)
The title spirocyclic ketones, possessing possible substitution patterns 1,4-dithiaspirodecan-6-one (1a), -7-one (3a), and -8-one (5a) and 1,5-dithiaspiroundecan-7-one (2a), -8-one (4a), and -9-one (6a), have been reduced with new strains of yeast (Saccharomyces cerevisiae, JCM 1819 and JCM 2214).Reductions of the prochiral ketones 1a-4a occur with high enantiofacial selectivity on the preparative scale (up to 99percent ee).The product alcohols (1,4-dithiaspirodecan-6-ol (1b) and -7-ol (3b) and 1,5-dithiaspiroundecan-7-ol (2b) and -8-ol (4b)) have theS configuration, as confirmed by 2D COSY experiments of the (S)-MTPA ester of 1b-4b using the configuration correlation model of Mosher.
