30355-60-3 Usage
Uses
Used in Pharmaceutical Synthesis:
6-(CHLOROMETHYL)-N-PHENYL-1,3,5-TRIAZINE-2,4-DIAMINE is used as a key intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic benefits.
Used in Dye Production:
In the dye industry, 6-(CHLOROMETHYL)-N-PHENYL-1,3,5-TRIAZINE-2,4-DIAMINE is utilized as a reactive intermediate, playing a crucial role in the creation of various dyes that have specific color characteristics and properties.
Used in Organic Synthesis:
6-(CHLOROMETHYL)-N-PHENYL-1,3,5-TRIAZINE-2,4-DIAMINE serves as a versatile building block in organic synthesis, enabling the formation of a wide range of organic compounds for different applications.
Used in Medical Research:
6-(CHLOROMETHYL)-N-PHENYL-1,3,5-TRIAZINE-2,4-DIAMINE is used as a subject of study in medical research for its potential to treat various diseases such as diabetes, inflammation, and cancer, due to its unique biochemical interactions.
Check Digit Verification of cas no
The CAS Registry Mumber 30355-60-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,3,5 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 30355-60:
(7*3)+(6*0)+(5*3)+(4*5)+(3*5)+(2*6)+(1*0)=83
83 % 10 = 3
So 30355-60-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H10ClN5/c11-6-8-14-9(12)16-10(15-8)13-7-4-2-1-3-5-7/h1-5H,6H2,(H3,12,13,14,15,16)
30355-60-3Relevant academic research and scientific papers
Synthesis and antiviral activity of benzimidazolyl-and triazolyl-1,3,5- triazines
Maarouf, Azza R.,Farahat, Abdelbasset A.,Selim, Khalid B.,Eisa, Hassan M.
, p. 703 - 710 (2012/09/22)
A novel series of 1,3,5-triazine analogs was successfully synthesized through conjugation with benzimidazole or 1,2,4-triazole derivatives via a methylenethio linker. The new analogs were in vitro evaluated against HSV-1 in Vero cells; among these analogs, two compounds exhibited good effect in inhibiting HSV-1 replication (for compound 5p: EC50 = 3.5 μg/ml, SI = 358; for compound 5r: EC50 = 5.0 μg/ml, SI = 300) in comparison to acyclovir. Springer Science+Business Media, LLC 2011.
