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  • Product NamePrednisone 21-acetate
  • CasNo. 125-10-0
  • MFC23H28O6
  • MW400.472
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Product Details

CasNo： 125-10-0

MF： C23H28O6

Factory Supply Industrial Grade Prednisone 21-acetate 125-10-0 with Best Price

  • Molecular Formula:C23H28O6
  • Molecular Weight:400.472
  • Vapor Pressure:5.69E-16mmHg at 25°C 
  • Melting Point:240-242°C (dec.) 
  • Refractive Index:1.579 
  • Boiling Point:582 °C at 760 mmHg 
  • PKA:12.31±0.60(Predicted) 
  • Flash Point:200.2 °C 
  • PSA：97.74000 
  • Density:1.28 g/cm3 
  • LogP:2.33660 

Prednisone 21-acetate(Cas 125-10-0) Usage

InChI:InChI=1/C23H28O6/c1-13(24)29-12-19(27)23(28)9-7-17-16-5-4-14-10-15(25)6-8-21(14,2)20(16)18(26)11-22(17,23)3/h6,8,10,16-17,20,28H,4-5,7,9,11-12H2,1-3H3/t16?,17?,20?,21?,22?,23-/m0/s1

125-10-0 Relevant articles

-

Herzog et al.

, p. 4781,4783 (1955)

-

Epoxidation of 1,4-dienyl 3-keto steroidal compounds by dimethyldioxirane: Kinetics

Navarro-Eisenstein, Angela M.,Vasquez, Pedro C.,Franklin, Paul J.,Baumstark

, p. 575 - 578 (2003)

The epoxidation of 1,4-dienyl 3-keto ste...

o-Iodoxybenzoic acid in dimethylformamide as a convenient reagent for the oxidation of alcohols to aldehydes and ketones

Lapitskaya, Margarita A.,Vasiljeva, Ljudmila L.,Pivnitsky, Kasimir K.

, p. 309 - 311 (2008)

DMF dissolves o-iodoxybenzoic acid (up t...

Preparation method of prednisone

-

Paragraph 0012; 0029; 0031; 0033; 0035; 0037; 0039, (2021/03/05)

The invention discloses a preparation me...

9-site dehalogenation preparation method of 9-halogenated steroid hormone compound

-

Paragraph 0029-0031, (2020/07/15)

The invention discloses a 9-site dehalog...

A by the 3,17-dione steroid preparing steroid the synthetic method of the compound of

-

Paragraph 0102; 0103; 0148-0153, (2017/03/14)

The invention discloses a synthetic meth...

Pyridinium o-iodoxybenzoate as a safe form of a famous oxidant

Kumanyaev, Ivan M.,Lapitskaya, Margarita A.,Vasiljeva, Ljudmila L.,Pivnitsky, Kasimir K.

experimental part, p. 129 - 131 (2012/09/05)

The stable pyridinium salt of o-iodoxybe...

125-10-0 Process route

prednisolone 21-acetate
52-21-1

prednisolone 21-acetate

(8S,9S,10R,11S,13S,14S)-11-Hydroxy-10,13-dimethyl-7,8,9,10,11,12,13,14,15,16-decahydro-6H-cyclopenta[a]phenanthrene-3,17-dione
898-84-0

(8S,9S,10R,11S,13S,14S)-11-Hydroxy-10,13-dimethyl-7,8,9,10,11,12,13,14,15,16-decahydro-6H-cyclopenta[a]phenanthrene-3,17-dione

prednisone acetate
125-10-0

prednisone acetate

Conditions
Conditions Yield
Product distribution; Rate constant; Irradiation; radiolytic degradation;
prednisolone 21-acetate
52-21-1

prednisolone 21-acetate

prednisone acetate
125-10-0

prednisone acetate

Conditions
Conditions Yield
With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In N,N-dimethyl-formamide; at 23 - 25 ℃; for 5h;
99%
With 1-hydroxy-1.oxo-1H-1λ5-benzo[d][1,2]iodoxol-3-one pyridinium salt; In N,N-dimethyl-formamide; at 24 - 28 ℃; for 4h;
97%
With N-bromoacetamide;
With chromium(VI) oxide;

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    acetic anhydride

125-10-0 Downstream products

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    6677-19-6

    17α,21-diacetoxypregna-1,4-diene-3,11,20-trione

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    82423-35-6

    21-acetoxypregna-1,4,16-triene-3,11,20-trione

  • 52-21-1
    52-21-1

    prednisolone 21-acetate

  • 14411-14-4
    14411-14-4

    1α,1β,17α-Trihydroxy-21-acetoxy-A-nor-Δ3(5)-pregnentrion-(2,11,20)

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