67146-22-9 Usage
Uses
Used in Coordination Chemistry:
5-Mercapto-1H-tetrazole-1-methane sulphonic acid is used as a ligand for [forming stable complexes with metal ions] due to its strong acidic properties and ability to chelate a wide range of metal ions, which is crucial in the study and synthesis of coordination compounds.
Used in Organometallic Synthesis:
In organometallic synthesis, 5-Mercapto-1H-tetrazole-1-methane sulphonic acid is used as a reagent for [its capacity to form stable organometallic complexes], contributing to the development of new materials and catalysts.
Used in Analytical Chemistry:
5-Mercapto-1H-tetrazole-1-methane sulphonic acid is used as a reagent for [determining various metal ions in solution], leveraging its chelating properties to enhance the accuracy and efficiency of metal ion analysis.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Mercapto-1H-tetrazole-1-methane sulphonic acid is used as a building block or intermediate for [the synthesis of pharmaceutical compounds], owing to its reactivity and potential to form diverse chemical structures.
Used in Electronics Industry:
5-Mercapto-1H-tetrazole-1-methane sulphonic acid is used as a material or component in [electronic devices or systems], potentially due to its ability to form complexes with metals used in electronic components.
Used in Agriculture:
In agriculture, 5-Mercapto-1H-tetrazole-1-methane sulphonic acid is used as a component in [agricultural chemicals or as a tool in soil analysis], taking advantage of its reactivity and complexing abilities to improve crop management or soil health.
Check Digit Verification of cas no
The CAS Registry Mumber 67146-22-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,1,4 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 67146-22:
(7*6)+(6*7)+(5*1)+(4*4)+(3*6)+(2*2)+(1*2)=129
129 % 10 = 9
So 67146-22-9 is a valid CAS Registry Number.
InChI:InChI=1/C2H4N4O3S2/c7-11(8,9)1-6-2(10)3-4-5-6/h1H2,(H,3,5,10)(H,7,8,9)
67146-22-9Relevant academic research and scientific papers
7-Acyl-3-(sulfonic acid and sulfamoyl substituted tetrazolyl thiomethyl) cephalosporins
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, (2008/06/13)
The compounds of this invention are cephalosporins having a 3- or 4-aminomethylphenylacetamido substituent at the 7-position and a sulfonic acid substituted tetrazolyl thiomethyl group at the 3-position of the cephem nucleus. The compounds have antibacterial activity.
Derivatives of 7-(2-substituted-2-hydroxyiminoacetamido)-3-(1-substituted tetrazol-5-ylthiomethyl-3-cephem-4-carboxylic acid
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, (2008/06/13)
New semisynthetic cephalosporins are described whose structures are characterized by having an α-oxyimino group in the 7-acetamido moiety and a sulfosubstituted tetrazolylthiomethyl group at position 3. The compounds are active antibacterial agents especially against Gram negative organisms.
7-Acyl-3-(sulfonic acid and sulfamoyl substituted tetrazolyl thiomethyl) cephalosporins
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, (2008/06/13)
The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and a sulfonic acid or sulfamoyl substituted tetrazolyl thiomethyl group at the 3-position of the cephem nucleus. The compounds have antibacterial activity.
7-Acyl-3-(sulfonic acid and sulfamoyl substituted tetrazolyl thiomethyl)cephalosporins
-
, (2008/06/13)
The compounds of this invention are cephalosporins having various acyl substituents at the 7-position and a sulfonic acid or sulfamoyl substituted tetrazolyl thiomethyl group at the 3-position of the cephem nucleus and intermediates for the preparation thereof. The 7-acylated compounds have antibacterial activity.
