81581-13-7 Usage
Chemical structure
Contains a triazole ring, a carboxylic acid group, and a thioether substituent attached to the triazole ring.
Molecular weight
Approximately 253.26 g/mol
Functional groups
Triazole, carboxylic acid, and thioether
Medicinal chemistry
Building block for the synthesis of pharmaceuticals and bioactive molecules.
Coordination chemistry
Used as a ligand in the development of metal-organic frameworks.
Pharmacological properties
May exhibit antimicrobial, anticancer, and other pharmacological properties.
Research and development
Of interest for further research and development in the field of drug discovery.
Solubility
Soluble in polar solvents such as water, methanol, and dimethyl sulfoxide (DMSO).
Stability
Generally stable under normal laboratory conditions, but sensitive to strong acids and bases.
Safety precautions
Handle with care, as it may have potential toxic effects. Use appropriate personal protective equipment (PPE) and follow proper disposal procedures.
Check Digit Verification of cas no
The CAS Registry Mumber 81581-13-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,5,8 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 81581-13:
(7*8)+(6*1)+(5*5)+(4*8)+(3*1)+(2*1)+(1*3)=127
127 % 10 = 7
So 81581-13-7 is a valid CAS Registry Number.
81581-13-7Relevant academic research and scientific papers
COMPOUNDS AND METHODS FOR TREATING OXALATE-RELATED DISEASES
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Paragraph 0248; 0292; 0294, (2019/09/12)
Disclosed herein are compounds and compositions for modulating glycolate oxidase, useful for treating oxalate-related diseases, such as hyperoxaluria, where modulating glycolate oxidase is expected to be therapeutic to a patent in need thereof. Methods of modulating glycolate oxidase activity in a human or animal subject is also provided.
Studies of v-Triazoles. Part 4. The 4-Methoxybenzyl Group, a Versatile N-Protecting Group for the Synthesis of N-Unsubstituted v-Triazoles
Buckle, Derek R.,Rockell, Caroline J.M.
, p. 627 - 630 (2007/10/02)
A series of readily prepared monocyclic N-(4-methoxybenzyl)-v-trizoles (1) have been converted into their N-unsubstituted derivatives (2) by treatment with trifluoroacetic acid at 65 deg C.The procedure allows the synthesis of a range of N-unsubstituted v
