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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)-

1,4-Benzodioxin, 6,7-dibromo-2,3-dihydro-

Brc1cc2OCCOc2cc1Br Request for Quotation
Chemical Name: 1,4-Benzodioxin, 6,7-dibromo-2,3-dihydro-
CAS Number: 25812-80-0
Product Number: AG003N0S(AGN-PC-0KKJWO)
Synonyms:
MDL No:
Molecular Formula: C8H6Br2O2
Molecular Weight: 293.9400

Identification/Properties

Properties
MP:
139.6-140.0℃
BP:
314.3°C at 760 mmHg
Storage:
Keep in dry area;Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
293.942g/mol
XLogP3:
3
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
0
Exact Mass:
293.871g/mol
Monoisotopic Mass:
291.873g/mol
Topological Polar Surface Area:
18.5A^2
Heavy Atom Count:
12
Formal Charge:
0
Complexity:
147
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:
Signal Word:
Warning
UN#:
N/A
Hazard Statements:
H302
Precautionary Statements:
P280-P305+P351+P338
Class:
N/A
Packing Group:
N/A

NMR Spectrum

Other Analytical Data

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Chemical Structure


6,7-dibromo-2,3-dihydro-1,4-benzodioxin is a versatile compound that finds several important applications in chemical synthesis. One of its key uses is as a building block in the creation of novel organic molecules with interesting properties. This compound can serve as a key intermediate in the synthesis of biologically active compounds, pharmaceuticals, and agrochemicals. Its unique structure and reactivity make it a valuable tool for organic chemists looking to design and create complex molecules for various applications. In addition, 6,7-dibromo-2,3-dihydro-1,4-benzodioxin can be utilized in the development of new materials, such as polymers and ligands, due to its ability to participate in a variety of chemical reactions. Its presence in a synthesis scheme can enable the synthesis of diverse compounds with tailored properties and functions.