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  2. Spiro[4H,8H-[1,4]dioxepino[2,3-g]indole-8,7'(8'H)-[5H,6H-5a,9a](iminomethano)[1H]cyclopent[f]indolizin]-10'-one,2',3',8'a,9,9',10-hexahydro-1'-hydroxy-1',4,4,8',8',11'-hexamethyl-,(1'R,5'aS,7'R,8'aS,9'aR)-

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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)-

Spiro[4H,8H-[1,4]dioxepino[2,3-g]indole-8,7'(8'H)-[5H,6H-5a,9a](iminomethano)[1H]cyclopent[f]indolizin]-10'-one,2',3',8'a,9,9',10-hexahydro-1'-hydroxy-1',4,4,8',8',11'-hexamethyl-,(1'R,5'aS,7'R,8'aS,9'aR)-

CN1C(=O)[C@]23C[C@@H]4[C@]1(CN2CC[C@@]3(C)O)C[C@]1(C4(C)C)CNc2c1ccc1c2OC=CC(O1)(C)C Request for Quotation
Chemical Name: Spiro[4H,8H-[1,4]dioxepino[2,3-g]indole-8,7'(8'H)-[5H,6H-5a,9a](iminomethano)[1H]cyclopent[f]indolizin]-10'-one,2',3',8'a,9,9',10-hexahydro-1'-hydroxy-1',4,4,8',8',11'-hexamethyl-,(1'R,5'aS,7'R,8'aS,9'aR)-
CAS Number: 187865-22-1
Product Number: AG00ANR9(AGN-PC-0QGXGK)
Synonyms:
MDL No: MFCD13195549
Molecular Formula: C28H37N3O4
Molecular Weight: 479.6111

Identification/Properties

Computed Properties
Molecular Weight:
479.621g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
6
Rotatable Bond Count:
0
Exact Mass:
479.278g/mol
Monoisotopic Mass:
479.278g/mol
Topological Polar Surface Area:
74.3A^2
Heavy Atom Count:
35
Formal Charge:
0
Complexity:
1010
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
5
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


Derquantel is a versatile compound that finds wide applications in chemical synthesis. In the field of organic chemistry, Derquantel is utilized as a powerful reagent for promoting various transformations. Its unique structure and reactivity make it particularly effective in facilitating complex reactions and forming intricate chemical bonds. By acting as a catalyst or reactant, Derquantel can accelerate the synthesis of valuable compounds and intermediates. Its compatibility with a range of functional groups allows for diverse applications in the construction of pharmaceuticals, agrochemicals, and materials. Additionally, Derquantel's selectivity and efficiency contribute to the success of synthetic pathways, enabling chemists to achieve desired products with high yields and purity. Such attributes make Derquantel an invaluable tool for advancing research and innovation in the realm of chemical synthesis.