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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)-

Estra-1,3,5(10)-triene-3,6,17-triol, (6a,17b)-

Oc1ccc2c(c1)[C@@H](O)C[C@@H]1[C@@H]2CC[C@]2([C@H]1CC[C@@H]2O)C Request for Quotation
Chemical Name: Estra-1,3,5(10)-triene-3,6,17-triol, (6a,17b)-
CAS Number: 1229-24-9
Product Number: AG000JRF(AGN-PC-0O0IVK)
Synonyms:
MDL No:
Molecular Formula: C18H24O3
Molecular Weight: 288.3814

Identification/Properties

Computed Properties
Molecular Weight:
288.387g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
3
Hydrogen Bond Acceptor Count:
3
Rotatable Bond Count:
0
Exact Mass:
288.173g/mol
Monoisotopic Mass:
288.173g/mol
Topological Polar Surface Area:
60.7A^2
Heavy Atom Count:
21
Formal Charge:
0
Complexity:
411
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


In chemical synthesis, (6S,8S,9S,13S,14S,17S)-13-methyl-6,7,8,9,11,12,14,15,16,17-decahydrocyclopenta[a]phenanthrene-3,6,17-triol serves as a versatile building block for the creation of complex organic compounds. Its unique structure allows for strategic manipulation of functional groups and stereochemistry, making it a valuable intermediate in the synthesis of various pharmaceuticals, natural products, and bioactive molecules. This compound can be utilized in the construction of steroid derivatives, hormone analogs, and other biologically active substances through selective chemical transformations and reactions.