42242-05-7 Usage
Uses
Used in Organic Synthesis:
2-aminopyridine-3-carbothioamide serves as a building block in the production of various pharmaceuticals and agrochemicals. Its unique chemical structure allows it to be a versatile component in the synthesis of a wide range of compounds with diverse applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 2-aminopyridine-3-carbothioamide is used as a key intermediate for the synthesis of drugs with potential therapeutic effects. Its presence in the molecular structure of certain drugs can contribute to their pharmacological properties.
Used in Agrochemical Industry:
Similarly, in the agrochemical industry, 2-aminopyridine-3-carbothioamide is utilized as a precursor in the synthesis of various agrochemicals, such as pesticides and herbicides, which are essential for agricultural productivity and crop protection.
Used in Antimicrobial Applications:
2-aminopyridine-3-carbothioamide has been studied for its antimicrobial properties, making it a potential candidate for use in applications that require the inhibition of microbial growth, such as in the development of antimicrobial agents for medical or environmental purposes.
Used in Anticancer Research:
Furthermore, 2-aminopyridine-3-carbothioamide has shown potential anticancer properties, indicating its use in the development of novel anticancer drugs. Its incorporation into drug molecules could contribute to the inhibition of cancer cell growth and the enhancement of existing cancer treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 42242-05-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,4 and 2 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 42242-05:
(7*4)+(6*2)+(5*2)+(4*4)+(3*2)+(2*0)+(1*5)=77
77 % 10 = 7
So 42242-05-7 is a valid CAS Registry Number.
42242-05-7Relevant academic research and scientific papers
Catalyst-free synthesis of 2-aryl-1,2-dihydro-quinazolin-4(1H)-thiones from 2-aminobenzothio-amides and aldehydes in water
Oschatz, Stefan,Brunzel, Tom,Wu, Xiao-Feng,Langer, Peter
, p. 1150 - 1158 (2015/08/03)
2-Dihydroquinazolin-4(1H)-thiones were prepared in up to excellent yields from 2-aminobenzothioamides and aldehydes. The reaction is carried out in water without the use of any catalyst or promoter. The sulfur-containing substrate can be obtained easily by thiation of the corresponding nitrile by solid sodium hydrosulfide.
PYRIDINE DERIVATIVE SUBSTITUTED BY HETEROARYL RING, AND ANTIFUNGAL AGENT COMPRISING THE SAME
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Page/Page column 78-79, (2009/06/27)
The present invention provides an antifungal agent that has excellent antifungal action, and is also excellent in terms of its properties, safety, and metabolic stability. The present invention discloses a compound represented by the following formula I or a salt thereof, and an antifungal agent comprising the compound or the salt: wherein R1 represents a hydrogen atom, a halogen atom, an amino group, a C1-6 alkyl group, a C1-6 alkoxy group, or a C1-6-alkoxy-C1-6-alkyl group; R2 represents a hydrogen atom or an amino group; X, Y, Z, and W independently represent a nitrogen atom, an oxygen atom, a sulfur atom, or -CH-, provided that at least two among X, Y, and W are nitrogen atoms; the ring A represents a 5- or 6-membered heteroaryl ring or a benzene ring; Q represents a methylene group, an oxygen atom, -CH2O-, -OCH2-, -NH-, -NHCH2-, or -CH2NH-; and R3 represents a C1-6 alkyl group, a C3-8 cycloalkyl group, a C6-10 aryl group, or a 5- or 6-membered heteroaryl group, each of which may have one or two substituents.
