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1-(4-amino-anilino)-anthraquinone is a chemical compound with the molecular formula C17H13N3O2. It is an anthraquinone derivative, characterized by the presence of an anthraquinone core, which is a tricyclic aromatic system consisting of two benzene rings fused to a central pyrone ring. The compound features a 4-aminoaniline group attached to the anthraquinone structure, which contributes to its chemical properties. This specific arrangement of atoms and functional groups endows 1-(4-amino-anilino)-anthraquinone with unique characteristics, making it a potentially useful intermediate in the synthesis of various dyes, pigments, and other chemical products.

2944-15-2

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2944-15-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2944-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,9,4 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2944-15:
(6*2)+(5*9)+(4*4)+(3*4)+(2*1)+(1*5)=92
92 % 10 = 2
So 2944-15-2 is a valid CAS Registry Number.

2944-15-2Relevant academic research and scientific papers

Anthracene derivatives as anti-cancer agents

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, (2008/06/13)

Use of compound of Formula (I): at least one of R1, R2, R5 and R6 is a group —AB and the others are independently selected from hydrogen, hydroxy, alkoxy or acyloxy, a group —AB a group -amino-(R7)nX—Y wherein R7 is a divalent organic radical and n is 0 or 1; R3 and R4are independently oxo, hydroxy or hydrogen; the or each A is independently a spacer group of formula -amino-(R7)n—X— which is bonded to the anthracene ring via the amino group nitrogen and to B via —X—, X is independently selected from O, NH and C(O); B is an amino acid residue or a peptide group or isostere thereof and Y is hydrogen or a capping group, or a physiologically acceptable derivative of such compound for the manufacture of a medicament for the treatment of cancers or microbial infections having cells exhibiting topoisomerase I activity characterised in that the group -amino-(R7)n—X— incorporates an optionally substituted heterocyclic ring directly attached to the anthroquinone ring through an amino nitrogen in the heterocycclic ring, or an optionally substituted heterocyclic or carbocyclic ring that is spaced from the anthraquinone ring by no more than an amino nitrogen and up to four carbon atoms.

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