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  2. 5a,8-Methano-5aH-cyclohepta[5,6]naphtho[2,1-b]furan-7-methanol,3b,4,5,7,8,9,10,10a,10b,11,12-dodecahydro-7-methoxy-10b-methyl-,(3bS,5aS,7R,8R,10aR,10bS)-

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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)-

5a,8-Methano-5aH-cyclohepta[5,6]naphtho[2,1-b]furan-7-methanol,3b,4,5,7,8,9,10,10a,10b,11,12-dodecahydro-7-methoxy-10b-methyl-,(3bS,5aS,7R,8R,10aR,10bS)-

CO[C@]1(CO)C[C@@]23C[C@H]1CC[C@H]3[C@]1([C@H](CC2)c2ccoc2CC1)C Request for Quotation
Chemical Name: 5a,8-Methano-5aH-cyclohepta[5,6]naphtho[2,1-b]furan-7-methanol,3b,4,5,7,8,9,10,10a,10b,11,12-dodecahydro-7-methoxy-10b-methyl-,(3bS,5aS,7R,8R,10aR,10bS)-
CAS Number: 108214-28-4
Product Number: AG0094E5(AGN-PC-0OY707)
Synonyms:
MDL No:
Molecular Formula: C21H30O3
Molecular Weight: 330.4611

Identification/Properties

Computed Properties
Molecular Weight:
330.468g/mol
XLogP3:
3.8
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
2
Exact Mass:
330.219g/mol
Monoisotopic Mass:
330.219g/mol
Topological Polar Surface Area:
42.6A^2
Heavy Atom Count:
24
Formal Charge:
0
Complexity:
521
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
6
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


Known for its versatile applications in chemical synthesis, 16-O-Methylcafestol is a potent compound that serves as a key reagent in various reactions. This unique molecule plays a crucial role in the construction of complex organic structures due to its ability to participate in a wide range of transformations. Whether used as a catalyst in asymmetric synthesis or as a building block in the preparation of bioactive compounds, this compound demonstrates remarkable efficacy and selectivity. Chemists rely on 16-O-Methylcafestol to facilitate challenging bond formations, including carbon-carbon and carbon-heteroatom bonds, making it an indispensable tool in modern synthetic chemistry. Its structural features offer distinct advantages in promoting desired regioselectivity and stereoselectivity, allowing for the efficient creation of intricate molecular architectures. Through its strategic incorporation into synthetic pathways, 16-O-Methylcafestol enables the rapid and efficient generation of valuable molecules with diverse applications across various industries.