75220-48-3 Usage
Uses
Used in Pharmaceutical Industry:
(4-CHLORO-PHENYL)-(5-METHYL-4,5-DIHYDRO-THIAZOL-2-YL)-AMINE is used as a building block for the synthesis of biologically active molecules due to its diverse chemical properties and reactivity. It has the potential for use in the development of new drugs, contributing to the advancement of pharmaceutical research and innovation.
Used in Agrochemical Industry:
In the agrochemical industry, (4-CHLORO-PHENYL)-(5-METHYL-4,5-DIHYDRO-THIAZOL-2-YL)-AMINE is used as a starting material for the development of new agrochemicals. Its unique chemical structure allows for the creation of compounds with specific pesticidal, herbicidal, or fungicidal properties, enhancing crop protection and yield.
Used in Materials Science:
(4-CHLORO-PHENYL)-(5-METHYL-4,5-DIHYDRO-THIAZOL-2-YL)-AMINE is used as a polymer additive or a reactive intermediate in the synthesis of functional materials. Its incorporation into polymers can improve their properties, such as stability, durability, or conductivity, making it a valuable component in the development of advanced materials for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 75220-48-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,5,2,2 and 0 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 75220-48:
(7*7)+(6*5)+(5*2)+(4*2)+(3*0)+(2*4)+(1*8)=113
113 % 10 = 3
So 75220-48-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H11ClN2S/c1-7-6-12-10(14-7)13-9-4-2-8(11)3-5-9/h2-5,7H,6H2,1H3,(H,12,13)/t7-/m1/s1
75220-48-3Relevant academic research and scientific papers
Synthesis, characterization, and antibacterial activity of some thiazoles derived from allyl thioureas
Khare,Sharma,Sharma
, p. 702 - 707 (2016/06/01)
Synthesis of thiazoles was carried out from allyl thioureas using different cyclizing agents such as hydrogen chloride gas and bromine. Synthesized compounds were characterized by IR, 1H and 13C NMR, mass spectrometry, and elemental analysis. The synthesized thiazoles were evaluated for their antibacterial activity against Gram postitive (Lactobacillus bulgaris and Streptococcus mitis) and Gram negative (Yersinia) as well as antifungal activity against Aspergillus niger fungi.