629652-21-7 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 9 carbon (C), 9 hydrogen (H), 7 nitrogen (N), and 1 sulfur (S) atoms.
Explanation
The compound belongs to the triazolo-thiadiazole class of compounds, which are characterized by the presence of a triazole ring and a thiadiazole ring in their structure.
Explanation
The triazole ring is a part of the compound's structure, consisting of three nitrogen atoms and two carbon atoms, forming a five-membered ring.
Explanation
The thiadiazole ring is another part of the compound's structure, consisting of two nitrogen atoms and three sulfur atoms, forming a five-membered ring.
Explanation
The compound is a primary amine, which means it has an amino group (-NH2) attached to the molecule.
Explanation
The compound is substituted at the 3-position with a 3-methylphenyl group, which is a phenyl group (a six-membered ring with alternating single and double bonds) with a methyl group (-CH3) attached to the third carbon atom.
Explanation
The compound is used in various fields, including medicinal chemistry research and drug development, due to its potential biological activities and pharmacological properties.
Explanation
While the compound is known to have potential biological activities, the specific activities are not provided in the material.
Explanation
The compound is mentioned to have pharmacological properties, but the specific properties are not provided in the material.
Class
Triazolo-thiadiazole
Triazole Ring
A five-membered ring with three nitrogen atoms and two carbon atoms
Thiadiazole Ring
A five-membered ring with two nitrogen atoms and three sulfur atoms
Primary Amine
Contains an amino group (-NH2)
Substitution
3-(3-methylphenyl) group
Applications
Medicinal chemistry research and drug development
Potential Biological Activities
Unknown specific activities
Pharmacological Properties
Unknown specific properties
Check Digit Verification of cas no
The CAS Registry Mumber 629652-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,9,6,5 and 2 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 629652-21:
(8*6)+(7*2)+(6*9)+(5*6)+(4*5)+(3*2)+(2*2)+(1*1)=177
177 % 10 = 7
So 629652-21-7 is a valid CAS Registry Number.
629652-21-7Relevant academic research and scientific papers
Condensed heterocyclic systems containing bridgehead nitrogen atom: Synthesis and bioactivity of imidazo[2, 1-b]-1,3,4-thiadiazolo[2,3-c]-s-triazoles, s-triazolo-[3,4-b]-1,3,4-thiadiazolo[3,2-b]imidazo[4,5-b] quinoxaline and bis-(s-triazolo[3,4-b]-1,3,4-thiadiazolo[3,2-b] [imidazo[4,5-b]cyclohexane]-5a, 6a-diene)
Mohan, Jag,Kumar, Ashok
, p. 1463 - 1466 (2007/10/03)
Condensation of 4-amino-5-mercapto-3-(m-methylphenyl)-s-triazole 1 with cyanogen bromide gives 6-amino-3-(m-methylphenyl)-s-triazolo[3,4-b]-1,3,4-thiadiazole 2 which on condensation with chloranil yields 3.9-di-(m-methylphenyl)-6,14-diaxo-bis-(s-triazolo[3,4-b]-1,3,4-thiadiazolo[3, 2-b][imidazo[4.5-b]cyclohexane]-5a. 6a-diene) 3. 3-(m-Methylphenyl)-s-triazolo[3,4-b]-1,3,4-thiadiazolo[3,2-b]imidazo[4,5-b] quinoxaline 4 is obtained by a similar condensation of 2 with 2,3-dichloroquinoxaline. The reaction of 2 with α-haloketones followed by bromination affords 7-aryl-3-(m-methylphenyl) imidazo[2,1-b]-1,3,4-thiadiazolo[2,3-c]-s-triazoles 5 and their 6-bromo analogues 6 respectively. The antibacterial and antifungal activities of some of the compounds have also been evaluated.
