7114-31-0 Usage
General Description
1-Morpholin-4-yl-anthraquinone is a chemical compound that belongs to the anthraquinone family. It is a synthetic organic compound that contains a morpholine group, which is a cyclic amine, attached to an anthraquinone molecule. This chemical is commonly used as a dye intermediate and in the production of pigments. It is also utilized in the manufacturing of pharmaceuticals, particularly as an intermediate in the synthesis of potential therapeutic agents. The presence of the morpholine group in this compound imparts unique properties and reactivity, making it valuable in various industrial applications. Additionally, 1-morpholin-4-yl-anthraquinone may also have potential uses in the field of organic synthesis and materials science.
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 articles and documents
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.
