52160-51-7 Usage
Uses
Used in Pharmaceutical Industry:
(1-METHYL-1H-PYRROL-2-YL)METHANOL, 97% is used as a key intermediate for the synthesis of various pharmaceuticals due to its ability to contribute to the development of novel drug molecules with potential therapeutic effects.
Used in Agrochemical Industry:
In the agrochemical sector, (1-METHYL-1H-PYRROL-2-YL)METHANOL, 97% serves as a crucial component in the production of agrochemicals, aiding in the creation of compounds that can enhance crop protection and yield.
Used as a Reagent in Chemical Synthesis:
(1-METHYL-1H-PYRROL-2-YL)METHANOL, 97% is utilized as a reagent in various chemical synthesis processes, facilitating the formation of complex organic molecules for research and industrial applications.
Used in Research and Development:
(1-METHYL-1H-PYRROL-2-YL)METHANOL,97% is also employed in research and development settings to explore new methods of synthesis and to investigate its potential in creating innovative materials and compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 52160-51-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,2,1,6 and 0 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 52160-51:
(7*5)+(6*2)+(5*1)+(4*6)+(3*0)+(2*5)+(1*1)=87
87 % 10 = 7
So 52160-51-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H9NO/c1-7-4-2-3-6(7)5-8/h2-4,8H,5H2,1H3
52160-51-7Relevant academic research and scientific papers
Microwave-assisted Cannizzaro reaction—Optimisation of reaction conditions
Janczewski, ?ukasz,Walczak, Ma?gorzata,Fr?czyk, Justyna,Kamiński, Zbigniew J.,Kolesińska, Beata
supporting information, p. 3290 - 3300 (2019/11/05)
The microwave-assisted Cannizzaro reaction was studied in order to develop fully reproducible synthetic protocols for transformation of aldehydes to carboxylic acid and alcohols. Optimised were the following process parameters: power, temperature, and time. Aromatic, heteroaromatic and aliphatic aldehydes were used in the studies. It was found that furfural, thiophene-2-carbaldehyde, pyridinecarboxaldehyde and aromatic aldehydes react under mild conditions, while 1-methyl-pyrrole-2-carboxaldehyde derivatives and aliphatic aldehydes require more drastic reaction conditions and a longer exposure time to microwave radiation.
