1. Home
  2. Pregna-1,4-diene-3,20-dione, 17,21-dihydroxy-

Contact Angene

Tel: +852 8191 6999

Email: [email protected]

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)-

Pregna-1,4-diene-3,20-dione, 17,21-dihydroxy-

OCC(=O)[C@@]1(O)CC[C@@H]2[C@]1(C)CC[C@H]1[C@H]2CCC2=CC(=O)C=C[C@]12C Request for Quotation
Chemical Name: Pregna-1,4-diene-3,20-dione, 17,21-dihydroxy-
CAS Number: 1807-14-3
Product Number: AG00ADSM(AGN-PC-0O544E)
Synonyms:
MDL No:
Molecular Formula: C21H28O4
Molecular Weight: 344.44462

Identification/Properties

Computed Properties
Molecular Weight:
344.451g/mol
XLogP3:
2.7
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
2
Exact Mass:
344.199g/mol
Monoisotopic Mass:
344.199g/mol
Topological Polar Surface Area:
74.6A^2
Heavy Atom Count:
25
Formal Charge:
0
Complexity:
692
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

Request for Quotation

Customer Feedback

Chemical Structure


11-Deoxy Prednisolone is a powerful intermediate compound utilized in chemical synthesis processes. With its unique structure and reactivity, this compound plays a crucial role in the creation of various pharmaceuticals, particularly corticosteroids. Its absence of a hydroxyl group at the 11th position distinguishes it from Prednisolone, opening up opportunities for specific modifications and reactions during synthesis. By strategically incorporating 11-Deoxy Prednisolone into synthetic pathways, chemists can access a wide range of derivatives with altered pharmacological properties, making it an indispensable tool in the pharmaceutical industry. Additionally, its controlled use in chemical transformations allows for the efficient and precise production of diverse steroid-based medications with enhanced therapeutic efficacy.