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  2. 3-Oxa-9-azoniatricyclo[3.3.1.02,4]nonane,7-[(hydroxydi-2-thienylacetyl)oxy]-9,9-dimethyl-, bromide,(1a,2b,4b,5a,7b)-

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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)-

3-Oxa-9-azoniatricyclo[3.3.1.02,4]nonane,7-[(hydroxydi-2-thienylacetyl)oxy]-9,9-dimethyl-, bromide,(1a,2b,4b,5a,7b)-

O=C(C(c1cccs1)(c1cccs1)O)OC1C[C@@H]2[C@@H]3[C@H]([C@H](C1)[N+]2(C)C)O3.[Br-] Request for Quotation
Chemical Name: 3-Oxa-9-azoniatricyclo[3.3.1.02,4]nonane,7-[(hydroxydi-2-thienylacetyl)oxy]-9,9-dimethyl-, bromide,(1a,2b,4b,5a,7b)-
CAS Number: 136310-93-5
Product Number: AG0011M7(AGN-PC-0PKW3S)
Synonyms:
MDL No:
Molecular Formula: C19H22BrNO4S2
Molecular Weight: 472.4163

Identification/Properties

Computed Properties
Molecular Weight:
472.412g/mol
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
5
Exact Mass:
471.017g/mol
Monoisotopic Mass:
471.017g/mol
Topological Polar Surface Area:
116A^2
Heavy Atom Count:
27
Formal Charge:
0
Complexity:
564
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
4
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
2
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (1α,2β,4β,5α,7β)-7-[(Hydroxydi-2-thienylacetyl)oxy]-9,9-di-methyl-3-oxa-9-azoniatricyclo[3.3.1.0]nonane bromide, commonly referred to as $name$, is a versatile reagent frequently employed in chemical synthesis. This compound serves as a crucial building block in organic synthesis due to its unique structural features and reactivity.In chemical synthesis, $name$ is utilized as a powerful acylating agent, enabling the introduction of the hydroxydi-2-thienylacetyl group onto various nucleophilic substrates. This acyl group serves as a key functional moiety in the formation of diverse organic compounds, including pharmaceuticals, natural products, and specialty chemicals.Moreover, the bromide moiety present in $name$ offers strategic opportunities for subsequent transformations through nucleophilic substitution reactions. This allows for further derivatization to tailor the properties of the target molecules, making $name$ a valuable tool in the synthesis of complex organic scaffolds.Overall, the application of (1α,2β,4β,5α,7β)-7-[(Hydroxydi-2-thienylacetyl)oxy]-9,9-di-methyl-3-oxa-9-azoniatricyclo[3.3.1.0]nonane bromide in chemical synthesis showcases its significance as a versatile reagent for the construction of intricate molecular structures with potential implications across various scientific fields.