79172-41-1 Usage
Uses
Used in Organic Synthesis:
(2-Nitrophenyl)(4-nitrophenyl)methanone is used as a versatile intermediate in organic synthesis for the preparation of various biologically active compounds and pharmaceuticals. Its unique structure allows for the creation of a wide range of organic compounds with potential applications in various industries.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, (2-Nitrophenyl)(4-nitrophenyl)methanone is used as a building block for the synthesis of various drugs. Its ability to form a wide range of organic compounds makes it a valuable component in the development of new medications.
Used in Dye and Pigment Production:
(2-Nitrophenyl)(4-nitrophenyl)methanone may also be used in the production of dyes, pigments, and other specialty chemicals. Its yellow crystalline solid form and chemical properties make it suitable for use in these applications, contributing to the color and properties of various products.
Check Digit Verification of cas no
The CAS Registry Mumber 79172-41-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,1,7 and 2 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 79172-41:
(7*7)+(6*9)+(5*1)+(4*7)+(3*2)+(2*4)+(1*1)=151
151 % 10 = 1
So 79172-41-1 is a valid CAS Registry Number.
79172-41-1Relevant academic research and scientific papers
Synthesis of Functionalized Ketones from Acid Chlorides and Organolithiums by Extremely Fast Micromixing
Nagaki, Aiichiro,Sasatsuki, Kengo,Ishiuchi, Satoshi,Miuchi, Nobuyuki,Takumi, Masahiro,Yoshida, Jun-ichi
supporting information, p. 4946 - 4950 (2019/03/21)
Synthesis of ketones containing various functional groups from acid chlorides bearing electrophilic functional groups and functionalized organolithiums was achieved using a flow microreactor system. Extremely fast mixing is important for high chemoselectivity.
Ozone-mediated Nitration of Aromatic Ketones and Related Compounds with Nitrogen Dioxide
Suzuki, Hitomi,Murashima, Takashi
, p. 903 - 908 (2007/10/02)
Alkyl aryl ketones react smoothly with nitrogen dioxide at low temperatures in the presence of ozone to give ortho- and meta-nitro derivatives as the principal products, the former usually being predominant (ortho:meta = 1.1-3.8:1.0).No attack was observed on the alkyl side chains.
