15121-86-5 Usage
Molecular weight
179.17 g/mol This is the mass of one mole of the compound, measured in grams.
Synthetic intermediate This indicates that the compound is used in organic synthesis to produce other chemicals.
4-nitrophenyl group attached to the second carbon of the prop-2-en-1-ol chain
This describes the structure of the compound, with a nitro group (-NO2) attached to a phenyl ring (a six-carbon ring with three hydrogen atoms replaced by a carbon-carbon double bond) on the second carbon of a propenol (an alcohol with a carbon-carbon double bond).
Nitroalkene
This is a type of organic compound that contains a nitro group (-NO2) and a carbon-carbon double bond.
Electron-withdrawing nitro group
The nitro group is electron-withdrawing, meaning it attracts electrons towards itself. This can affect the reactivity and chemical properties of the compound.
Possible uses in pharmaceuticals, agricultural chemicals, and other industrial applications
This indicates the potential applications of the compound in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 15121-86-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,1,2 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15121-86:
(7*1)+(6*5)+(5*1)+(4*2)+(3*1)+(2*8)+(1*6)=75
75 % 10 = 5
So 15121-86-5 is a valid CAS Registry Number.
15121-86-5Relevant academic research and scientific papers
SUBSTITUTED PYRAZOLYL-BASED CARBOXAMIDE AND UREA DERIVATIVES BEARING A PHENYL MOIETY SUBSTITUTED WITH AN O-CONTAINING GROUP AS VANILLOID RECEPTOR LIGANDS
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Page/Page column 144; 145, (2013/05/23)
The invention relates to substituted pyrazolyl-based carboxamide and urea derivatives of formula (Q) as vanilloid receptor ligands, to pharmaceutical compositions containing these compounds and also to these compounds for use in the treatment and/or prophylaxis of pain and further diseases and/or disorders.
Electrogenerated Base (EG Base) Induced Hydroxymethylation of the Side Chain of Nitroalkylbenzenes with Paraformaldehyde
Torii, Sigeru,Murakami, Yasuo,Tanaka, Hideo,Okamoto, Koichi
, p. 3143 - 3147 (2007/10/02)
Hydroxymethylation of nitroalkylbenzenes with paraformaldehyde was accomplished by electrolysis in a (CH2O)n-DMF-Et4NOTs-(Pt electrode) system.The reaction was found to be catalytic (0.25 faraday/mol) and dependent on the electroreduction of formaldehyde and/or nitroalkylbenzene.A variety of nitroalkylbenzenes were transformed to their corresponding mono- and/or bishydroxymethylated derivatives in good yield.The product yield and selectivity were shown to depend on the order of reagent addition, solvent, supporting electrolyte, and structure of the starting nitroalkylbenzenes.A plausible mechanism of the generation of base catalysts (EG base) in electroreductive media is discussed.
