100805-84-3 Usage
Chemical structure
A compound consisting of a urea group attached to a phenyl and tetrazole group.
Urea group
A common functional group in many biologically active compounds.
Phenyl ring
An aromatic ring that can contribute to the compound's stability and reactivity.
Tetrazole ring
A five-membered ring with four nitrogen atoms, often associated with biological activity.
Methoxy group
An electron-donating group that can influence the compound's reactivity and pharmacological properties.
Sulfanyl-acetyl group
A functional group that can contribute to the compound's reactivity and potential pharmacological properties.
Potential applications
Medicinal or biological applications due to its unique structure and functional groups.
Biological activity
The presence of the methoxy group on the phenyl ring and the tetrazole ring indicates potential biological activity, as these structural motifs are often associated with medicinal chemistry.
Reactivity
The sulfanyl-acetyl group attached to the tetrazole ring can contribute to the compound's reactivity, which may be important for its potential pharmacological properties.
Pharmacological properties
The unique structure and functional groups of this compound suggest that it may have potential pharmacological properties, although further research would be needed to determine its specific effects and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 100805-84-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,8,0 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 100805-84:
(8*1)+(7*0)+(6*0)+(5*8)+(4*0)+(3*5)+(2*8)+(1*4)=83
83 % 10 = 3
So 100805-84-3 is a valid CAS Registry Number.
100805-84-3Relevant articles and documents
Synthesis and AChE Activity of 2--N-carbonyl>acetamides
Sen Gupta, Anil K.,Bhattacharya, Tapas,Rastogi, Anita
, p. 578 - 579 (2007/10/02)
A number of 2--N-carbonyl>acetamides (III) have been synthesised by the condensation of 1-aryl-1H-tetrazol-5-thiol (I) with 1-chloro-N-carbonyl>acetamides (II), and evaluated for their acetylcholinesterase (AChE) inhibitory activity.
