38237-76-2 Usage
Description
4-aminohexanoylphenone, also known as 4-AHPK, is a chemical compound commonly used in the manufacturing of pharmaceuticals and organic synthesis. It is a ketone derivative with a six-carbon chain containing an amino group and a phenyl group. 4-AHPK is often utilized as a starting material for the production of various heterocyclic compounds and as a building block for the synthesis of new drugs. It has been studied for its potential in anti-tumor and anti-inflammatory activities, as well as its ability to inhibit enzymes involved in pathological processes. Additionally, 4-aminohexanoylphenone has shown promise in the development of new chemical entities and drug candidates. Despite its potential therapeutic uses, further research is needed to fully understand the biological and pharmacological properties of this chemical.
Uses
Used in Pharmaceutical Industry:
4-aminohexanoylphenone is used as a starting material for the production of various heterocyclic compounds and as a building block for the synthesis of new drugs. Its potential in anti-tumor and anti-inflammatory activities, as well as its ability to inhibit enzymes involved in pathological processes, make it a promising candidate for the development of new chemical entities and drug candidates.
Used in Organic Synthesis:
4-aminohexanoylphenone is used as a key intermediate in the synthesis of various organic compounds. Its unique structure with a six-carbon chain containing an amino group and a phenyl group allows for versatile chemical reactions and the formation of a wide range of products.
Used in Drug Development:
4-aminohexanoylphenone is used in the development of new chemical entities and drug candidates. Its potential therapeutic uses in anti-tumor and anti-inflammatory activities, as well as its enzyme inhibitory properties, make it a valuable compound for further research and development in the pharmaceutical industry.
Check Digit Verification of cas no
The CAS Registry Mumber 38237-76-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,2,3 and 7 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 38237-76:
(7*3)+(6*8)+(5*2)+(4*3)+(3*7)+(2*7)+(1*6)=132
132 % 10 = 2
So 38237-76-2 is a valid CAS Registry Number.
InChI:InChI=1/C12H17NO/c1-2-3-4-5-12(14)10-6-8-11(13)9-7-10/h6-9H,2-5,13H2,1H3
38237-76-2Relevant articles and documents
Preparation method of aryl ketone compound
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Paragraph 0041-0049; 0061-0065; 0067, (2022/04/16)
The invention provides a preparation method of an aryl ketone compound, and belongs to the technical field of compound synthesis. The method comprises the following steps: under the action of a silver catalyst and water, carrying out reaction on aryl alkyne with a structure as shown in a formula 1 in a solvent at 60-120 DEG C for 12-48 hours, and separating and purifying a product after the reaction is finished, so as to obtain the single aryl ketone compound with a structure as shown in a formula I, the raw materials are easy to obtain, the experimental operation is simple, the yield of the prepared single aryl ketone compound is good, and gram-scale experiments can be carried out.
Palladium-catalysed transfer hydrogenation of aromatic nitro compounds - An unusual chain elongation
Németh, János,Kiss, árpád,Hell, Zoltán
, p. 6094 - 6096 (2013/10/22)
Aromatic nitro compounds are reduced via transfer hydrogenation in the presence of palladium on magnesium-lanthanum mixed oxide support in ethanol yielding the corresponding amines. With several acetophenone derivatives, the reduction was accompanied by c
Rapid microwave assisted hydration of internal arylalkynes in the presence of PTSA: an efficient regioselective access to carbonyl compounds
Le Bras, Ga?lle,Provot, Olivier,Peyrat, Jean-Fran?ois,Alami, Mouad,Brion, Jean-Daniel
, p. 5497 - 5501 (2007/10/03)
A metal-free procedure for the regioselective hydration of internal arylalkynes under microwave irradiation is described. The reaction promoted by PTSA takes place rapidly in EtOH and regioselectively afforded in good yields various carbonyl compounds 2.