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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)-

Estrogens, conjugated

O=C1CC[C@@H]2[C@@H]1CC[C@H]1C2=CCc2c1ccc(c2)OS(=O)(=O)[O-].[Na+] Request for Quotation
Chemical Name: Estrogens, conjugated
CAS Number: 12126-59-9
Product Number: AG01DQ9J(AGN-PC-0PFIYO)
Synonyms:
MDL No: MFCD00240712
Molecular Formula: C17H17NaO5S
Molecular Weight: 356.36865

Identification/Properties

Computed Properties
Molecular Weight:
370.395g/mol
Hydrogen Bond Donor Count:
0
Hydrogen Bond Acceptor Count:
5
Rotatable Bond Count:
2
Exact Mass:
370.085g/mol
Monoisotopic Mass:
370.085g/mol
Topological Polar Surface Area:
91.9A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
682
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
3
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


Conjugated Estrogen, also known as Premarin, is a mixture of estrogens derived from the urine of pregnant mares. In chemical synthesis, Conjugated Estrogen plays a crucial role in the development of various pharmaceuticals and hormone replacement therapies. Its unique chemical structure and properties make it a valuable component in the synthesis of estrogen-based medications and formulations, particularly in the treatment of menopausal symptoms. Conjugated Estrogen is utilized as a key starting material in the synthesis of selective estrogen receptor modulators (SERMs) and other hormone-related drugs. Its ability to mimic the endogenous estrogen in the human body makes it a versatile compound for creating pharmaceuticals that target estrogen receptors and hormonal imbalance. Additionally, Conjugated Estrogen is employed in the production of hormone replacement therapies that alleviate symptoms associated with menopause and hormonal deficiencies. Its role in chemical synthesis extends to the creation of novel estrogenic compounds with improved bioavailability and therapeutic efficacy. By serving as a foundational building block in drug development, Conjugated Estrogen drives advancements in the pharmaceutical industry and enhances the quality of hormone-based treatments.