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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)-

1,3,2-Benzodioxabismole-5-carboxylic acid, 2,7-dihydroxy-

O[Bi]1Oc2c(O1)cc(cc2O)C(=O)O Request for Quotation
Chemical Name: 1,3,2-Benzodioxabismole-5-carboxylic acid, 2,7-dihydroxy-
CAS Number: 99-26-3
Product Number: AG003ODZ(AGN-PC-0OP3DC)
Synonyms:
MDL No:
Molecular Formula: C7H5BiO6
Molecular Weight: 394.0914

Identification/Properties

Properties
MP:
223 °C (dec.)(lit.)
BP:
501.1°C at 760 mmHg
Storage:
Inert atmosphere;Room Temperature;
Form:
Solid
Solubility:
Practically insoluble in water and in ethanol (96 per cent). It dissolves in mineral acids with decomposition and in solutions of alkali hydroxides, producing a reddishbrown liquid.

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


$1,3,2-Benzodioxabismole-5-carboxylic acid, 2,7-dihydroxy- is a key compound utilized in chemical synthesis for its versatile applications. In organic chemistry, it serves as a building block for the synthesis of complex molecules and pharmaceuticals. Due to its unique structural features, this compound can participate in a variety of reactions, including cross-coupling reactions, nucleophilic additions, and cycloadditions, leading to the formation of diverse chemical compounds. Its distinct molecular architecture allows for precise control over regioselectivity and stereochemistry in synthetic processes. Researchers and chemists rely on the utility of 1,3,2-Benzodioxabismole-5-carboxylic acid, 2,7-dihydroxy- to facilitate the creation of novel materials and biologically active substances, making it an indispensable tool in the realm of chemical synthesis.