104070-63-5 Usage
Explanation
The compound is composed of 16 carbon atoms, 16 hydrogen atoms, 4 nitrogen atoms, and 1 sulfur atom.
Explanation
The compound is a derivative of the 1,3,4-thiadiazole ring, which is a five-membered ring containing sulfur and nitrogen atoms.
Explanation
The compound contains a hydrazino group (-NH-NH2) and a phenylmethyl group (-CH2Ph) attached to the thiadiazole ring.
Explanation
Due to its diverse biological activities, the compound has potential use in the development of drugs and agrochemicals.
Explanation
Some studies have shown that derivatives of the compound exhibit antibacterial, antifungal, and antitumor activities, making it a subject of interest in drug discovery and development.
Explanation
While the compound has shown promise in various biological activities, more research is required to fully understand its potential applications and toxicity.
Chemical Structure
1,3,4-Thiadiazole derivative
Functional Groups
Hydrazino and phenylmethyl groups
Potential Applications
Pharmaceuticals and agrochemicals
Biological Activities
Antibacterial, antifungal, and antitumor properties
Research Status
Further research needed
Check Digit Verification of cas no
The CAS Registry Mumber 104070-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,0,7 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104070-63:
(8*1)+(7*0)+(6*4)+(5*0)+(4*7)+(3*0)+(2*6)+(1*3)=75
75 % 10 = 5
So 104070-63-5 is a valid CAS Registry Number.
104070-63-5Relevant academic research and scientific papers
Substituted 1,3,4-Thiadiazoles with Anticonvulsant Activity. 1. Hydrazines
Chapleo, Christopher B.,Myers, Malcolm,Myers, Peter L.,Saville, John F.,Smith, Alan C. B.,et al.
, p. 2273 - 2280 (2007/10/02)
The synthesis and anticonvulsant activity of a series of 2-aryl-5-hydrazino-1,3,4-thiadiazoles are described.The combination of preferred aromatic substituents in the 2-position coupled with alkyl substitution on the hydrazine moiety led to a number of potent compounds lacking sedation, ataxia, or lethality. 5-(2-Biphenylyl)-2-(1-methylhydrazino)-1,3,4-thiadiazole (4m) represents a new class of anticonvulsant agent and compares favorably with the standard drugs phenytoin, phenobarbital, and carbamazepine.
