7114-31-0 Usage
Uses
Used in Dye and Pigment Production:
1-Morpholin-4-yl-anthraquinone is used as a dye intermediate for the synthesis of various dyes, contributing to the coloration and stability of pigments in different industries.
Used in Pharmaceutical Manufacturing:
1-Morpholin-4-yl-anthraquinone serves as an intermediate in the synthesis of potential therapeutic agents, playing a crucial role in the development of new pharmaceuticals.
Used in Organic Synthesis and Materials Science:
Due to its unique properties and reactivity, 1-Morpholin-4-yl-anthraquinone may have potential applications in the field of organic synthesis and materials science, where it can be utilized to create new compounds and materials with specific characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 7114-31-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,1 and 4 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7114-31:
(6*7)+(5*1)+(4*1)+(3*4)+(2*3)+(1*1)=70
70 % 10 = 0
So 7114-31-0 is a valid CAS Registry Number.
InChI:InChI=1/C18H15NO3/c20-17-12-4-1-2-5-13(12)18(21)16-14(17)6-3-7-15(16)19-8-10-22-11-9-19/h1-7H,8-11H2
7114-31-0Relevant academic research and scientific papers
Synthesis of 9-chloro-1,10-anthraquinone and its reactions with amines
Gorelik,Titova,Gladysheva
, p. 1141 - 1146 (2007/10/03)
1-Dichlorophosphoryloxy-9,9-dichloroanthrone, a product of the reaction between 1-hydroxyanthraquinone and PCl5, reacts with primary amines in benzene to give first 1-(diaminophosphoryloxy)-9,9-dichloroanthrones and then the corresponding 9-imines. The reaction in DMF occurs with elimination of the phosphoryloxy group and generation of 9-chloro-1,10-anthraquinone that undergoes amination followed by substitution of the hydrogen atom in position 4 rather than a chlorine atom in position 9, which is the most active position in 2,4,9-trichloro-1,10-anthraquinone. The second step of amination results in 4,9-di(alkylamino)-1,10-anthraquinone. The literature data on obtaining individual 9-chloro-1,10-anthraquinone under the action of bases on 1-dichorophosphoryloxy-9,9-dichloroanthrone were not experimentally supported.
