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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)-

Betamethasone acetate

CC(=O)OCC(=O)[C@@]1(O)[C@H](C)C[C@@H]2[C@]1(C)C[C@H](O)[C@]1([C@H]2CCC2=CC(=O)C=C[C@]12C)F Request for Quotation
Chemical Name: Betamethasone acetate
CAS Number: 987-24-6
Product Number: AG005TZU(AGN-PC-0WAJBT)
Synonyms:
MDL No:
Molecular Formula: C24H31FO6
Molecular Weight: 434.4977

Identification/Properties

Properties
MP:
203-205°C
Storage:
2-8℃;
Form:
Solid
Computed Properties
Molecular Weight:
434.504g/mol
XLogP3:
2.8
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
7
Rotatable Bond Count:
4
Exact Mass:
434.21g/mol
Monoisotopic Mass:
434.21g/mol
Topological Polar Surface Area:
101A^2
Heavy Atom Count:
31
Formal Charge:
0
Complexity:
910
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
8
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


Betamethasone acetate is a synthetic corticosteroid commonly used in chemical synthesis for its potent anti-inflammatory and immunosuppressive properties. In the realm of organic chemistry, Betamethasone acetate serves as a crucial intermediate for the production of various pharmaceutical compounds. Its functional groups enable diverse chemical reactions, making it a versatile building block in the synthesis of more complex molecules. With its high level of reactivity, Betamethasone acetate is utilized in the creation of new drug candidates and formulations aimed at treating a wide range of medical conditions. Its role in chemical synthesis extends to the development of advanced drug delivery systems and the study of structure-activity relationships in medicinal chemistry. As a key component in the synthesis of pharmaceuticals, Betamethasone acetate plays an essential role in advancing the field of drug discovery and development.