92712-44-2 Usage
Molar mass
361.15 g/mol This is the mass of one mole of the compound, which is a measure of its size and can affect its physical and chemical properties.
Tetrazole derivative This refers to the compound's structure, which is based on a five-membered ring containing four nitrogen atoms and one carbon atom.
Substituted phenyl group This indicates that the compound has a phenyl group (a six-carbon ring with a hydrogen atom replaced by a different atom or group of atoms) as part of its structure.
Iodopropynyl group This is a halogenated alkyl group (a carbon-hydrogen chain) with an iodine atom attached to a propynyl group (a three-carbon chain with a triple bond between the first two carbons).
Building block for pharmaceuticals This suggests that the compound is commonly used as an intermediate in the synthesis of other pharmaceuticals and bioactive compounds.
Analgesic and anti-inflammatory properties This indicates that the compound has been studied for its potential to relieve pain and reduce inflammation, which are important pharmacological effects.
Valuable tool for drug discovery This suggests that the compound's unique structure and properties make it useful for research and development in the field of pharmaceutical science.
Check Digit Verification of cas no
The CAS Registry Mumber 92712-44-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,7,1 and 2 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 92712-44:
(7*9)+(6*2)+(5*7)+(4*1)+(3*2)+(2*4)+(1*4)=132
132 % 10 = 2
So 92712-44-2 is a valid CAS Registry Number.
92712-44-2Relevant academic research and scientific papers
Iodoallyl and iodopropargyl substituted tetrazoles and anti-microbial compositions thereof
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, (2008/06/13)
Triiodoallyl- or iodopropargyl-substituted tetrazole compounds which are prepared by reacting substituted tetrazole compound with reactive derivatives of corresponding triiodoallyl alcohol or iodopropargyl alcohol or by iodinating propargyltetrazole compo
