211388-16-8 Usage
Thiadiazole family
Heterocyclic compounds
The compound belongs to a class of heterocyclic compounds that contain a five-membered ring with sulfur and nitrogen atoms.
Acetyl group
A functional group derived from acetic acid
The presence of an acetyl group (-COCH3) in the compound contributes to its reactivity and potential applications in pharmaceuticals.
Amino group
A functional group containing nitrogen
The compound contains an amino group (-NH2), which can form hydrogen bonds and participate in various chemical reactions.
Potential building block
Synthesis of pharmaceuticals and biologically active molecules
Due to its unique structure, this compound can be used as a building block for the synthesis of various pharmaceuticals and biologically active molecules.
Pharmaceutical industry
Development of drugs targeting diseases and conditions
The compound has potential applications in the pharmaceutical industry for the development of drugs that target a range of diseases and conditions.
Research purposes
Study of heterocyclic chemistry and drug discovery
This compound is important for research purposes, as it can be used to study heterocyclic chemistry and contribute to the discovery of new drugs and therapeutic agents.
Chemical structure
1,3,4-Thiadiazol-2(3H)-one core with 3-acetyl and 5-amino substitutions
The core structure of the compound is a 1,3,4-thiadiazol-2(3H)-one, with a 3-acetyl group and a 5-amino group attached to the ring.
Chemical stability
Influenced by the presence of functional groups
The stability of the compound may be influenced by the presence of the acetyl and amino functional groups, which can participate in various chemical reactions.
Solubility
May vary depending on the solvent and environmental conditions
The solubility of the compound in different solvents (e.g., water, organic solvents) may vary and can be influenced by factors such as temperature and pH.
Check Digit Verification of cas no
The CAS Registry Mumber 211388-16-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,1,3,8 and 8 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 211388-16:
(8*2)+(7*1)+(6*1)+(5*3)+(4*8)+(3*8)+(2*1)+(1*6)=108
108 % 10 = 8
So 211388-16-8 is a valid CAS Registry Number.
211388-16-8Relevant articles and documents
Acylation of 5-amino-3H-1,3,4-thiadiazolin-2-one
Ra, Do Young,Cho, Nam Sook,Cho, Jae Too
, p. 525 - 530 (2007/10/03)
Acylation of 5-amino-3H-1,3,4-thiadiazolin-2-one (2) was undertaken selectively at either the 3-NH position or at 5-amino group depending on reaction conditions. The 3-NH is highly acidic and acylation takes place with acid anhydrides at this position in
Mass Spectrometric Studies of 3-Substituted-5-amino-1,3,4-thiadiazolin-2-ones
Lee, Un Chul,Lee, Won,Kim, Yun Je,Park, Song Ja,Ra, Do Young,Cho, Nam Sook
, p. 201 - 210 (2007/10/03)
Fragment pathways of 3-alkyl and acyl-5-amino-1,3,4-thiadiazolin-2-ones were completely assigned by mass analyzed kinetic energy spectra (MIKE), collisional activated dissociation (CAD) spectra and high resolution mass spectra. + and + ions were directly formed from molecular ion of the 3-alkyl compounds and from 5-amino-3H-1,3,4-thiadiazolin-2-one ion (1) which was produced by McLafferty rearrangement from molecular ion of 3-acyl compounds.A loss of neutral SCO was only detected from 3-alkyl substituted molecular ions. - Keywords: 3-substituted-5-amino-1,3,4-thiadiazolin-2-ones; MIKE and CAD spetra
