28612-36-4 Usage
Description
(3Z,5Z)-3,5-bis(phenylmethylidene)tetrahydro-4H-thiopyran-4-one, also known as "Benzylidene tetrahydrothiopyran-4-one", is an organic compound with a complex molecular structure. It is a member of the tetrahydrothiopyran-4-one family, which are cyclic compounds containing a sulfur atom and a carbonyl group. This chemical is commonly used as a building block in organic synthesis and has potential applications in pharmaceuticals and agrochemicals.
Uses
Used in Pharmaceutical Industry:
(3Z,5Z)-3,5-bis(phenylmethylidene)tetrahydro-4H-thiopyran-4-one is used as a building block in organic synthesis for the development of new pharmaceutical compounds. Its unique molecular structure and potential antimicrobial, antiviral, and anticancer properties make it a promising candidate for the creation of novel therapeutic agents.
Used in Agrochemical Industry:
(3Z,5Z)-3,5-bis(phenylmethylidene)tetrahydro-4H-thiopyran-4-one is used as a building block in the synthesis of agrochemicals, such as pesticides and herbicides. Its potential antimicrobial and antiviral properties can contribute to the development of effective agents for crop protection and disease control in agriculture.
Check Digit Verification of cas no
The CAS Registry Mumber 28612-36-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,6,1 and 2 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 28612-36:
(7*2)+(6*8)+(5*6)+(4*1)+(3*2)+(2*3)+(1*6)=114
114 % 10 = 4
So 28612-36-4 is a valid CAS Registry Number.
28612-36-4Relevant articles and documents
A convenient one-pot synthesis of thiopyrano[4,3-b]pyran derivatives under LiOH·H2O/EtOH/ultrasonic conditions
Pourabdi, Ladan,Osati, Fatemeh,Mojtahedi, Mohammad M.,Abaee, Saeed M.
, p. 34 - 42 (2017/01/17)
Various derivatives of thiopyrano[4,3-b]pyran structure are synthesized via a multicomponent procedure starting from tetrahydro-4H-thiopyran-4-one, aromatic aldehydes, and malononitrile. Reactions take place by the use of catalytic quantities of LiOH·Hsu
