829-40-3 Usage
Uses
Used in Organic Synthesis:
1-(2-FLUOROPHENYL)-2-NITROPROPENE is used as a building block in organic synthesis for the creation of complex organic molecules. Its unique structure, featuring fluorophenyl and nitro groups, allows for a wide range of chemical reactions and the formation of diverse compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, 1-(2-FLUOROPHENYL)-2-NITROPROPENE is used as a precursor for the synthesis of various drugs. Its chemical properties make it a valuable component in the development of new medications with specific therapeutic effects.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, 1-(2-FLUOROPHENYL)-2-NITROPROPENE serves as a precursor for the synthesis of different agrochemicals, such as pesticides and herbicides, contributing to the development of effective solutions for agricultural challenges.
Safety Precautions:
Due to the potential hazards and toxicity associated with 1-(2-FLUOROPHENYL)-2-NITROPROPENE, its use and handling require adherence to strict safety protocols. This includes proper storage, handling, and disposal measures to minimize risks to human health and the environment.
Check Digit Verification of cas no
The CAS Registry Mumber 829-40-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 8,2 and 9 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 829-40:
(5*8)+(4*2)+(3*9)+(2*4)+(1*0)=83
83 % 10 = 3
So 829-40-3 is a valid CAS Registry Number.
InChI:InChI=1/C9H8FNO2/c1-7(11(12)13)6-8-4-2-3-5-9(8)10/h2-6H,1H3/b7-6+
829-40-3Relevant academic research and scientific papers
Substrate promiscuity of ortho-naphthoquinone catalyst: Catalytic aerobic amine oxidation protocols to deaminative cross-coupling and n-nitrosation
Kim, Hun Young,Oh, Kyungsoo,Si, Tengda
, p. 9216 - 9221 (2019/10/08)
ortho-Naphthoquinone-based organocatalysts have been identified as versatile aerobic oxidation catalysts. Primary amines were readily cross-coupled with primary nitroalkanes via deaminative pathway to give nitroalkene derivatives in good to excellent yields. Secondary and tertiary amines were inert to ortho-naphthoquinone catalysts; however, secondary nitroalkanes were readily converted by ortho-naphthoquinone catalysts to the corresponding nitrite species that in situ oxidized the amines to the corresponding N-nitroso compounds. Without using harsh oxidants in a stoichiometric amount, the present catalytic aerobic oxidation protocol utilizes the substrate promiscuity feature to provide a facile access to amine oxidation products under mild reaction conditions.
PROCESS FOR THE PREPARATION OF LACTAMS FROM GLYOXYLIC ACID
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Page/Page column 12, (2017/03/14)
A process for the synthesis of lactams suitable for use in antimicrobial, anti-biofilm bacteriostatic compositions.
Clean five-step synthesis of an array of 1,2,3,4-tetra-substituted pyrroles using polymer-supported reagents
Caldarelli, Marina,Habermann, Joerg,Ley, Steven V.
, p. 107 - 110 (2007/10/03)
Polymer-supported reagents and other solid sequestering agents may be used to generate an array of 1,2,3,4-tetra-substituted pyrrole derivatives without any chromatographic purification step.
