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  2. 9,10-Anthracenedione, 1,4-bis[[2-[(2-hydroxyethyl)amino]ethyl]amino]-

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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

9,10-Anthracenedione, 1,4-bis[[2-[(2-hydroxyethyl)amino]ethyl]amino]-

OCCNCCNc1ccc(c2c1C(=O)c1c(C2=O)cccc1)NCCNCCO Request for Quotation
Chemical Name: 9,10-Anthracenedione, 1,4-bis[[2-[(2-hydroxyethyl)amino]ethyl]amino]-
CAS Number: 64862-96-0
Product Number: AG00EIQ7(AGN-PC-0JK64T)
Synonyms:
MDL No:
Molecular Formula: C22H28N4O4
Molecular Weight: 412.4821

Identification/Properties

Properties
Storage:
-10 ℃;
Computed Properties
Molecular Weight:
412.49g/mol
XLogP3:
1.7
Hydrogen Bond Donor Count:
6
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
12
Exact Mass:
412.211g/mol
Monoisotopic Mass:
412.211g/mol
Topological Polar Surface Area:
123A^2
Heavy Atom Count:
30
Formal Charge:
0
Complexity:
513
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


1,4-Bis((2-((2-hydroxyethyl)amino)ethyl)amino)anthracene-9,10-dione, also known as $name$, plays a crucial role in chemical synthesis as a versatile intermediate compound. Its unique chemical structure allows for a wide range of applications in organic synthesis, particularly in the development of novel materials and pharmaceuticals.Its ability to undergo various chemical reactions, such as condensation, oxidation, and complexation reactions, makes it a valuable building block in the synthesis of organic compounds. In particular, $name$ is often used as a key component in the preparation of dyes, fluorescent probes, and bioactive molecules.Furthermore, the presence of hydroxyl and amino functional groups in $name$ provides opportunities for further derivatization, enabling chemists to tailor its properties for specific applications. Its compatibility with a variety of solvents and reaction conditions also enhances its utility in organic synthesis.Overall, the application of 1,4-Bis((2-((2-hydroxyethyl)amino)ethyl)amino)anthracene-9,10-dione in chemical synthesis highlights its importance as a versatile and valuable compound in the field of organic chemistry.