10486-42-7 Usage
Uses
Used in Pharmaceutical Industry:
2H-Naphth[2,3-d]imidazole-2-thione,1,3-dihydro-(9CI) is used as a potential building block for the synthesis of pharmaceutical compounds due to its unique heterocyclic structure, which may contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical field, 2H-Naphth[2,3-d]imidazole-2-thione,1,3-dihydro-(9CI) may be utilized as a component in the development of new pesticides or herbicides, leveraging its chemical structure to target and control agricultural pests and weeds more effectively.
Used in Materials Science:
2H-Naphth[2,3-d]imidazole-2-thione,1,3-dihydro-(9CI) is used as a precursor in the creation of advanced materials, potentially contributing to the development of new polymers, composites, or other materials with enhanced properties for various applications.
Used in Catalyst Development:
2H-Naphth[2,3-d]imidazole-2-thione,1,3-dihydro-(9CI) may also be used in the development of new catalysts, where its specific structural features could enable or enhance chemical reactions in industrial processes, leading to more efficient and sustainable chemical production methods.
Further research and studies are necessary to fully understand the properties and potential applications of 2H-Naphth[2,3-d]imidazole-2-thione,1,3-dihydro-(9CI), ensuring its safe and effective use across different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 10486-42-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,8 and 6 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 10486-42:
(7*1)+(6*0)+(5*4)+(4*8)+(3*6)+(2*4)+(1*2)=87
87 % 10 = 7
So 10486-42-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H8N2S/c14-11-12-9-5-7-3-1-2-4-8(7)6-10(9)13-11/h1-6H,(H2,12,13,14)
10486-42-7Relevant academic research and scientific papers
One-step construction of unsymmetrical thioureas and oxazolidinethiones from amines and carbon disulfide: Via a cascade reaction sequence
Ding, Chaochao,Wang, Shaoli,Sheng, Yaoguang,Dai, Qian,Zhao, Yunjie,Liang, Guang,Song, Zengqiang
, p. 26768 - 26772 (2019/09/06)
A concise and versatile method for the construction of unsymmetrical thioureas and oxazolidinethiones from amines and carbon disulfide has been achieved in DMSO without addition of extra reagents. The present protocol is compatible with various secondary amines and primary amines, and suitable for intermolecular and intramolecular reactions. Diverse unsymmetrical thioureas and oxazolidinethiones were efficiently obtained in good to excellent yields via a cascade reaction sequence.
Naphth[2,3-d]imidazoles
-
, (2008/06/13)
Imidazole derivatives of the formula STR1 wherein R1, R2, R3 R4, R5, X and n are as hereinafter set forth, and pharmaceutically acceptable acid addition salts thereof, are described. The compounds of formula I are useful in the treatment of gastric ulcers.
