6392-01-4 Usage
Description
(4-methoxyphenyl)(morpholin-4-yl)methanethione is a thioamide chemical compound that features a methoxyphenyl group and a morpholin-4-ylmethyl group attached to a methanethione functional group. (4-methoxyphenyl)(morpholin-4-yl)methanethione is of interest in medicinal chemistry and drug development due to its unique structural features and potential interactions with biological targets.
Uses
Used in Medicinal Chemistry:
(4-methoxyphenyl)(morpholin-4-yl)methanethione is used as a compound of interest for medicinal chemistry due to its potential interactions with biological targets and the presence of both methoxyphenyl and morpholin-4-ylmethyl groups.
Used in Drug Development:
(4-methoxyphenyl)(morpholin-4-yl)methanethione is used as a candidate in drug development for its potential biological activities, which may include antibacterial, antifungal, and antiviral properties, given the general properties of thioamides.
While the specific applications and uses of (4-methoxyphenyl)(morpholin-4-yl)methanethione are not well-documented, its structural features and the properties of thioamides suggest that it may have potential in various industries, particularly in the development of new pharmaceuticals and treatments. Further research and investigation are needed to explore its full potential and possible applications.
Check Digit Verification of cas no
The CAS Registry Mumber 6392-01-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,9 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6392-01:
(6*6)+(5*3)+(4*9)+(3*2)+(2*0)+(1*1)=94
94 % 10 = 4
So 6392-01-4 is a valid CAS Registry Number.
6392-01-4Relevant articles and documents
Ni-Catalyzed Synthesis of Thiocarboxylic Acid Derivatives
Monteith, John J.,Scotchburn, Katerina,Mills, L. Reginald,Rousseaux, Sophie A. L.
, p. 619 - 624 (2022/01/20)
A Ni-catalyzed cross-coupling of readily accessible O-alkyl xanthate esters or thiocarbonyl imidazolides and organozinc reagents for the synthesis of thiocarboxylic acid derivatives has been developed. This method benefits from a fast reaction time, mild reaction conditions, and ease of starting material synthesis. The use of transition-metal catalysis to access a diverse range of thiocarbonyl-containing compounds provides a useful complementary approach when compared with previously established methodologies.
Mixed bases mediated synthesis of thioamides in water
Li, Jiao,Ren, Xuanhe,Li, Ganzhong,Liang, Helong,Zhao, Yajie,Wang, Zhiwu,Li, Heng,Yuan, Bingxin
, p. 229 - 237 (2020/02/20)
A mixed bases mediated protocol is developed to synthesize thioamides from N-aryl or N-alkylamide, aldehyde and elemental sulfur in water. This reaction requires no addition of external oxidant and avoids large excess of amides. Various functional groups
Willgerodt-Kindler reaction at room temperature: Synthesis of thioamides from aromatic aldehydes and cyclic secondary amines
Kale, Arun D.,Tayade, Yogesh A.,Mahale, Sachin D.,Patil, Rahul D.,Dalal, Dipak S.
, (2019/09/12)
A simple method for the synthesis of thioamide derivatives in DMSO at room temperature and at 120 °C has been developed. Total 27 compounds were prepared under both conditions via a one-pot, three component reaction between substituted aromatic aldehydes,
