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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)-

3H-Phenoxazin-3-one, 4,6-di-1,3,2-dithiarsolan-2-yl-7-hydroxy-

Oc1ccc2c(c1[As]1SCCS1)oc1c(n2)ccc(=O)c1[As]1SCCS1 Request for Quotation
Chemical Name: 3H-Phenoxazin-3-one, 4,6-di-1,3,2-dithiarsolan-2-yl-7-hydroxy-
CAS Number: 438226-89-2
Product Number: AG00DFFT(AGN-PC-00PBT0)
Synonyms:
MDL No:
Molecular Formula: C16H13As2NO3S4
Molecular Weight: 545.3825

Identification/Properties

Properties
MP:
>144°C (dec.)
Storage:
-10 ℃;Inert atmosphere;Light sensitive;
Form:
Solid
Computed Properties
Molecular Weight:
545.367g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
8
Rotatable Bond Count:
2
Exact Mass:
544.821g/mol
Monoisotopic Mass:
544.821g/mol
Topological Polar Surface Area:
160A^2
Heavy Atom Count:
26
Formal Charge:
0
Complexity:
704
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

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound 3H-Phenoxazin-3-one, 4,6-di-1,3,2-dithiarsolan-2-yl-7-hydroxy is a versatile chemical reagent commonly used in chemical synthesis for its unique properties. Its presence in a reaction mixture can facilitate the formation of various organic compounds through its ability to act as a catalyst or a reactive intermediate.Given its specific structure, this compound can participate in a variety of chemical reactions, such as oxidation, reduction, and nucleophilic substitutions. It plays a crucial role in the synthesis of complex organic molecules by acting as a key building block or a functional group modifier.Furthermore, the 3H-Phenoxazin-3-one, 4,6-di-1,3,2-dithiarsolan-2-yl-7-hydroxy compound offers selectivity and efficiency in numerous transformations, making it an indispensable tool for chemists engaged in synthetic chemistry. Its presence in a reaction scheme can lead to the production of diverse and valuable chemical products with high yields and purity.