71969-32-9 Usage
Uses
Used in Pharmaceutical Industry:
(4-aminophenyl)(3,4-dimethoxyphenyl)methanone is used as an intermediate for the synthesis of various pharmaceuticals due to its analgesic and anti-inflammatory properties. It is a potential candidate for drug development, contributing to the creation of new medications for pain relief and inflammation management.
Used in Agrochemical Industry:
In the agrochemical industry, (4-aminophenyl)(3,4-dimethoxyphenyl)methanone is used as an intermediate for the synthesis of agrochemicals, which can be utilized in the development of pesticides, herbicides, and other agricultural products to improve crop yield and protect plants from pests.
Used in Organic Chemistry Research:
(4-aminophenyl)(3,4-dimethoxyphenyl)methanone is used as a reagent in research and laboratory settings for chemical reactions. Its unique structure allows it to participate in various organic synthesis processes, aiding scientists in the development of new organic molecules and compounds.
Used in Synthesis of Organic Compounds:
(4-aminophenyl)(3,4-dimethoxyphenyl)methanone is also used as a precursor for the synthesis of various organic molecules. Its versatility in chemical reactions makes it an important building block in the creation of complex organic structures, which can be applied in a wide range of industries, including pharmaceuticals, materials science, and chemical manufacturing.
Check Digit Verification of cas no
The CAS Registry Mumber 71969-32-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,9,6 and 9 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 71969-32:
(7*7)+(6*1)+(5*9)+(4*6)+(3*9)+(2*3)+(1*2)=159
159 % 10 = 9
So 71969-32-9 is a valid CAS Registry Number.
71969-32-9Relevant academic research and scientific papers
Synthesis, molecular modelling and biological evaluation of 4-amino-2(1H)-quinazolinone and 2,4(1H,3H)-quinazolidone derivatives as antitumor agents
Richter, Stephanie,Gioffreda, Barbara
, p. 810 - 820 (2012/03/08)
A series of 6-benzoyl-, 6-arylthio- and 6-arylsulfonyl-4-amino-2(1H)- quinazolinones and -2,4(1H,3H)-quinazolinediones were prepared. They were evaluated in vitro for their cytotoxicity against the NCI-60 cancer cell lines. A series of 6-benzoyl-, 6-arylthio- and 6-arylsulfonyl-4-amino-2(1H)- quinazolinones and -2,4(1H,3H)-quinazolinediones were prepared. They were evaluated in vitro for their cytotoxicity against the NCI-60 cancer cell lines. Copyright
Efficient one-pot Friedel-Crafts acylation of benzene and its derivatives with unprotected aminocarboxylic acids in polyphosphoric acid
Ivanov, Iliyan,Nikolova, Stoyanka,Statkova-Abeghe, Stela
, p. 1405 - 1411 (2007/10/03)
A number of aminobenzophenones have been synthesized by acylation of benzene and its derivatives with different 2-,3-,4-aminobenzoic and 4-aminophenyl-acetic acids in polyphosphoric acid via Friedel-Crafts reaction as compounds with expected antitumor activity. Copyright Taylor & Francis Group, LLC.
Immunotherapeutic agents
-
, (2008/06/13)
Cyano and carboxy derivatives of substituted styrenes are inhibitors of tumor necrosis factor α, nuclear factor κB, and phosphodiesterase and can be used to combat cachexia, endotoxic shock, retrovirus replication, asthma, and inflammatory conditions. A typical embodiment is 3,3-bis-(3,4-dimethoxyphenyl)acrylonitrile.
