89365-24-2 Usage
Chemical structure
A thiadiazole ring with two amine groups at positions 2 and 5, and an isopropyl group (1-methylethyl) attached to the nitrogen at position 1.
Application
Pharmaceutical industry
Use
Building block for the synthesis of various drugs and pharmaceutical compounds
Pharmacological activities
Antitumor, anti-inflammatory, and anticancer activities
Other uses
Intermediate in the manufacturing of agrochemicals and dyes
Attention
Diverse biological activities and potential therapeutic applications
Chemical classification
Heterocyclic compound
Functional groups
Thiadiazole ring, amine groups, and isopropyl group
Solubility
Not specified in the provided material
Stability
Not specified in the provided material
Reactivity
Not specified in the provided material
Toxicity
Not specified in the provided material
Environmental impact
Not specified in the provided material
Regulatory status
Not specified in the provided material
Check Digit Verification of cas no
The CAS Registry Mumber 89365-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,3,6 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89365-24:
(7*8)+(6*9)+(5*3)+(4*6)+(3*5)+(2*2)+(1*4)=172
172 % 10 = 2
So 89365-24-2 is a valid CAS Registry Number.
89365-24-2Relevant academic research and scientific papers
Reaction of 4-Alkyl/arylthiosemicarbazides with Cyanamide
Koshy, Lissamma,Joshua, C. P.
, p. 530 - 531 (2007/10/02)
The condensation of cyanamide with 4-alkyl/arylthiosemicarbazide hydrochlorides (I.HCl) results in the formation of 2-alkyl/arylamino-5-amino-1,3,4,-thiadiazoles (III) and 3-amino-4-alkyl/aryl-5-mercapto-1,2,4-triazoles (IV).
