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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)-

Pregna-5,16-dien-20-one, 3-hydroxy-, (3b)-

O[C@H]1CC[C@]2(C(=CC[C@@H]3[C@@H]2CC[C@]2([C@H]3CC=C2C(=O)C)C)C1)C Request for Quotation
Chemical Name: Pregna-5,16-dien-20-one, 3-hydroxy-, (3b)-
CAS Number: 1162-53-4
Product Number: AG000BW3(AGN-PC-0NYYM3)
Synonyms:
MDL No:
Molecular Formula: C21H30O2
Molecular Weight: 314.4617

Identification/Properties

Properties
MP:
205-210°C
Storage:
Room Temperature;
Form:
Solid
Computed Properties
Molecular Weight:
314.469g/mol
XLogP3:
3.9
Hydrogen Bond Donor Count:
1
Hydrogen Bond Acceptor Count:
2
Rotatable Bond Count:
1
Exact Mass:
314.225g/mol
Monoisotopic Mass:
314.225g/mol
Topological Polar Surface Area:
37.3A^2
Heavy Atom Count:
23
Formal Charge:
0
Complexity:
601
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

GHS Pictogram:
N/A
Signal Word:
UN#:
-
Hazard Statements:
-
Precautionary Statements:
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


16-Dehydropregnenolone, also known as 16-DPA, is a key intermediate in the synthesis of various steroid compounds. This versatile molecule plays a significant role in chemical synthesis by serving as a precursor for the production of important hormones such as progesterone and corticosteroids. In addition, 16-DPA can be utilized for the synthesis of novel steroid derivatives with potential pharmacological applications. Its structural properties make it a valuable building block for creating diverse steroid analogs with enhanced biological activities.eyond its role in hormone biosynthesis, 16-DPA is a valuable tool in the development of new pharmaceuticals and bioactive compounds. Its unique chemical structure and reactivity allow for the creation of custom-designed steroid molecules with specific properties and functions. Researchers in the field of medicinal chemistry and drug discovery often rely on 16-DPA as a starting material for the synthesis of potent and selective steroid-based drugs. By harnessing the synthetic versatility of 16-DPA, scientists can explore new avenues for improving drug efficacy, reducing side effects, and targeting specific biological pathways.