5429-28-7 Usage
Description
4-DIETHYLAMINOBENZOIC ACID, also known as 4-DEAB, is an organic compound with the molecular formula C11H13NO2. It is a derivative of benzoic acid, featuring a diethylamino group at the 4-position. 4-DIETHYLAMINOBENZOIC ACID is characterized by its ability to form various chemical bonds and participate in different chemical reactions, making it a versatile building block in the synthesis of various compounds.
Uses
Used in Pharmaceutical Industry:
4-DIETHYLAMINOBENZOIC ACID is used as a reactant for the preparation of amides by acylation of amines using (acyl)benzotriazoles. This application is particularly relevant in the synthesis of pharmaceutical compounds, as amides are common structural elements in many drugs and bioactive molecules. The use of 4-DEAB in this process allows for the creation of a diverse range of amide-containing compounds with potential therapeutic applications.
Used in Chemical Synthesis:
In the field of chemical synthesis, 4-DIETHYLAMINOBENZOIC ACID serves as a valuable intermediate for the production of various organic compounds. Its reactivity and functional group compatibility make it a useful building block for creating complex molecules with specific properties and applications. This includes the synthesis of dyes, pigments, and other specialty chemicals that require the unique structural features provided by 4-DEAB.
Used in Research and Development:
4-DIETHYLAMINOBENZOIC ACID is also utilized in research and development settings, where it can be employed as a starting material or a synthetic intermediate for the exploration of new chemical reactions and the development of novel compounds. Its versatility in participating in various chemical transformations makes it a valuable tool for chemists working on the design and synthesis of new molecules with potential applications in various industries, such as pharmaceuticals, materials science, and agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 5429-28-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,2 and 9 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 5429-28:
(6*5)+(5*4)+(4*2)+(3*9)+(2*2)+(1*8)=97
97 % 10 = 7
So 5429-28-7 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO2/c1-3-12(4-2)10-7-5-9(6-8-10)11(13)14/h5-8H,3-4H2,1-2H3,(H,13,14)/p-1
5429-28-7Relevant articles and documents
A Cross-linked Conjugated Polymer Photosensitizer Enables Efficient Sunlight-Induced Photooxidation
Wu, Wenbo,Xu, Shidang,Qi, Guobin,Zhu, Han,Hu, Fang,Liu, Zitong,Zhang, Deqing,Liu, Bin
supporting information, p. 3062 - 3066 (2019/01/25)
Photooxidation under sunlight has potential in organic synthesis, bacterial killing, and organic waste treatment. Photosensitizers (PSs) can play an important role in this process. High 1O2 generation efficiency and excellent photostability under sunlight, as well as easy recyclability are ideal properties for PSs, but are not easy to achieve simultaneously. Herein, a pure organic porous conjugated polymer PS, CPTF, shows great photostability, large specific surface area, and high 1O2 generation efficiency under sunlight for photooxidation. For the oxidation of aromatic aldehyde to aromatic acid, the PS catalyst shows excellent recyclability, and enables solvent-free reactions in high yields both under direct sunlight and simulated AM 1.5G irradiation. In addition, the successful application of CPTF as an antibacterial agent and organic waste decomposition under simulated AM 1.5G irradiation indicates the potential of CPTF in sunlight-induced waste water treatment.
A practical method for the preparation of 4-nitrogen-substituted benzoic acids
Shinozuka, Tsuyoshi,Nakao, Akira,Saito, Keiji,Naito, Satoru
, p. 1090 - 1091 (2007/10/03)
An efficient and practical method for the preparation of 4-nitrogen-substituted benzoic acids is described. Our method consists of the aromatic substitution of 2,2,2,4′-tetrafluoroacetophenone with amines, followed by haloform reaction to the benzoic acids. In this method, even though for the less nucleophilic 7-, 8-, and 9-membered amines 1 equiv. was used, corresponding benzoic acids were obtained in moderate to excellent yield. As the experimental procedure including purification is simple, this method is applicable to large-scale syntheses. Copyright
