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1-Thia-4-azaspiro[4.5]decan-3-one, 4-(4-chlorophenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65655-85-8

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65655-85-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65655-85-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,6,5 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 65655-85:
(7*6)+(6*5)+(5*6)+(4*5)+(3*5)+(2*8)+(1*5)=158
158 % 10 = 8
So 65655-85-8 is a valid CAS Registry Number.

65655-85-8Relevant academic research and scientific papers

Facile synthesis of spiro thiazolidinone via cyclic ketones, amines and thioglycolic acid by MCM-41-Schiff base-CuSO4·5H2O

Hui, Yonghai,Zhang, Yongfei,Luo, Yongyue,Li, Jianpeng,Wang, Yun,Gao, Tianming,Xia, Jialiang,Wang, Sheng,Zhang, Shiqi

, p. 521 - 532 (2020/10/19)

Mesoporous MCM-41-supported Schiff base and CuSO4?5H2O (MCM-41@Schiff base-CuSO4?5H2O) catalyzed one-pot three-component condensation of cyclic ketones, amines and thioglycolic acid in toluene. And a series of corresponding spiro thiazolidinone derivatives were obtained in high yields (up to 97%). The synthesized catalyst was characterized via FT-IR, XRD, SEM, TEM and EDS and can be easily recovered by centrifugation and reused at 10 times without any change in catalytic activity. Moreover, the scale-up experiment also demonstrated the practicability of the catalytic system on the condensation. The possible mechanisms pave the way to investigation on the reactions of other cyclic ketones with thioglycolic acid.

An efficient method for the transformation of 5-ylidenerhodanines into 2,3,5-trisubstituted-4-thiazolidinones

Kaminskyy, Danylo,Khyluk, Dmytro,Vasylenko, Olexandr,Lesyk, Roman

experimental part, p. 557 - 559 (2012/02/03)

The use of 3-substituted-2-mercaptoacrylic acids, synthesized via hydrolysis of 5-ylidenerhodanines for the preparation of 2,3,5-trisubstituted-4- thiazolidinones via a new variant of the one-pot, three-component reaction has been studied.

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