195-68-6 Usage
Uses
Used in Pharmaceutical Industry:
2,4-Diamino-6-mercaptopyrimidine serves as an essential building block in the synthesis of various pharmaceutical compounds. Its ability to chelate metal ions makes it particularly useful in the development of drugs that target metal-related disorders or that require metal ion coordination for their mechanism of action.
Used in Agrochemical Industry:
In the agrochemical sector, 2,4-Diamino-6-mercaptopyrimidine is utilized in the creation of herbicides. Its chemical properties allow for the design of compounds that can effectively control or kill unwanted plant species, thereby enhancing crop productivity and agricultural yields.
Used in Chemical Synthesis:
As an intermediate in chemical reactions, 2,4-Diamino-6-mercaptopyrimidine plays a crucial role in the synthesis of a wide array of organic and inorganic compounds. Its reactivity and functional groups facilitate its involvement in numerous chemical processes, contributing to the production of various chemical products.
Used in Metal Chelation Therapy:
2,4-Diamino-6-mercaptopyrimidine is employed as a chelating agent in medical applications, particularly for metal chelation therapy. Its strong affinity for metal ions aids in the treatment of heavy metal poisoning by safely removing toxic metals from the body.
Used in Anticancer Research:
2,4-Diamino-6-mercaptopyrimidine is also being explored for its potential as an anticancer agent. Its ability to inhibit the growth of tumor cells positions it as a candidate for further research into novel cancer treatments, with the aim of developing new therapeutic strategies to combat cancer.
Overall, 2,4-Diamino-6-mercaptopyrimidine's diverse applications across different industries underscore its significance in modern science and technology, with ongoing research likely to uncover additional uses and enhance its potential impact on various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 195-68-6 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 1,9 and 5 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 195-68:
(5*1)+(4*9)+(3*5)+(2*6)+(1*8)=76
76 % 10 = 6
So 195-68-6 is a valid CAS Registry Number.
InChI:InChI=1/C16H10S/c1-2-4-14-11(3-1)5-6-12-7-8-13-9-10-17-16(13)15(12)14/h1-10H
195-68-6Relevant academic research and scientific papers
Synthetic Utility of Arylmethylsulfones: Annulative π-Extension of Aromatics and Hetero-aromatics Involving Pd(0)-Catalyzed Heck Coupling Reactions
Sankar, Elumalai,Raju, Potharaju,Karunakaran, Jayachandran,Mohanakrishnan, Arasambattu K.
, p. 13583 - 13593 (2017/12/26)
A straightforward and general method for the synthesis of annulated thiophene, dibenzothiophene, and carbazoles analogues has been achieved involving alkylation of 2-bromo-1-(phenylsulfonylmethyl)arene/heteroarene with arylmethyl bromides/heteroarylmethyl bromides using t-BuOK as a base in DMF, followed by Pd(0)-mediated intramolecular Heck coupling in the presence of K2CO3 in DMF at 80-140 °C. The attractive feature of this protocol is that a wide variety of π-conjugated heterocycles could be readily accessed by an appropriate choice of arylmethylsulfones and benzylic bromides.
Synthesis of trans-dihydrodiol derivatives of phenanthro[3,4-b]-thiophene and phenanthro[4,3-b]thiophene
Kumar, Subodh,Saravanan, Srinivasan,Reuben, Peter,Kumar, Atul
, p. 1345 - 1355 (2007/10/03)
The present study describes the synthesis of phenanthro[3,4-b]thiophene (3), phenanthro[4,3-b]thiophene (4) and its potential dihydrodiol metabolites, trans-6,7-dihydroxy-6,7-dihydrophenanthro[3,4-b]thiophene (5) and trans-8,9-dihydroxy-8,9-dihydrophenant
