34930-31-9 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule of the compound.
Explanation
The compound contains a heterocyclic ring, which is a ring containing different types of atoms, in this case, sulfur and nitrogen.
Explanation
The compound has sulfur and nitrogen atoms in its structure, which are part of the heterocyclic ring.
Explanation
The compound has a methoxyphenylmethyl group, which is a benzene ring with a methoxy group (-OCH3) attached to it.
Explanation
The compound is used in the development and research of pharmaceuticals, potentially due to its unique structure and properties.
Explanation
The specific properties and potential applications of the compound may vary based on its exact structural features and the level of purity achieved during synthesis or purification.
Explanation
This is the IUPAC name of the compound, which provides a systematic way to identify and describe the structure of the molecule.
Heterocyclic amine
Yes
Contains sulfur and nitrogen atoms
Yes
Contains a methoxyphenylmethyl group
Yes
Pharmaceutical and research applications
Yes
Properties and uses depend on structure and purity
Yes
Check Digit Verification of cas no
The CAS Registry Mumber 34930-31-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,4,9,3 and 0 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 34930-31:
(7*3)+(6*4)+(5*9)+(4*3)+(3*0)+(2*3)+(1*1)=109
109 % 10 = 9
So 34930-31-9 is a valid CAS Registry Number.
34930-31-9Relevant academic research and scientific papers
An efficient protocol for the formation of aminothiatriazoles from thiocarbamoylimidazolium salts
Ponzo, Marisa G,Evindar, Ghotas,Batey, Robert A
, p. 7601 - 7604 (2007/10/03)
A new protocol for the formation of substituted aminothiatriazoles from thiocarbamoylimidazolium salts is outlined. Thiocarbamoylimidazolium salts are synthesized from the corresponding amines by treatment with thiocarbonyldiimidazole (TCDI) followed by methylation with iodomethane. Thiocarbamoylimidazolium salts are shown to act as thiocarbamoyl cation equivalents. Substitution of the salts by azide anion followed by electrocyclization affords substituted aminothiatriazoles in good to excellent yields.
