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11-DEHYDROCORTICOSTERONE


  • CAS
  • Purity
  • 72-23-1
  • 99%
Inquiry

Buy reliable Quality 11-DEHYDROCORTICOSTERONE 72-23-1 raw material with Honest Price

  • Molecular Formula: C21H28 O4
  • Molecular Weight: 344.451
  • Vapor Pressure: 1.9E-13mmHg at 25°C 
  • Melting Point: 183.5°C 
  • Refractive Index: 1.4430 (estimate) 
  • Boiling Point: 530°C at 760 mmHg 
  • PKA: 12.95±0.10(Predicted) 
  • Flash Point: 288.4°C 
  • PSA: 71.44000 
  • Density: 1.21g/cm3 
  • LogP: 2.87490 

11-DEHYDROCORTICOSTERONE(Cas 72-23-1) Usage

Definition

ChEBI: An 11-oxo steroid that is corticosterone in which the hydroxy substituent at the 11beta position has been oxidised to give the corresponding ketone.

InChI:InChI=1/C21H28O4/c1-20-8-7-13(23)9-12(20)3-4-14-15-5-6-16(18(25)11-22)21(15,2)10-17(24)19(14)20/h9,14-16,19,22H,3-8,10-11H2,1-2H3/t14-,15-,16+,19+,20-,21-/m0/s1

72-23-1 Relevant articles

Structure-dependent inhibition of human and rat 11β-hydroxysteroid dehydrogenase 2 activities by phthalates

Zhao, Binghai,Chu, Yanhui,Huang, Yadong,Hardy, Dianne O.,Lin, Shaoqiang,Ge, Ren-Shan

, p. 79 - 84 (2010)

Phthalates are diesters of phthalic acid...

Mass spectrometry imaging for dissecting steroid intracrinology within target tissues

Cobice, Diego F.,Logan MacKay,Goodwin, Richard J. A.,McBride, Andrew,Langridge-Smith, Patrick R.,Webster, Scott P.,Walker, Brian R.,Andrew, Ruth

, p. 11576 - 11584 (2014/01/06)

Steroid concentrations within tissues ar...

Efficient C-21 Deoxygenation of 21-Alkoxy-20-keto Corticoid Steroids with Trimethylsilyl Iodide in the Presence of Methanol

Nagaoka, Masao,Kunitama, Yurie,Numazawa, Mitsuteru

, p. 334 - 338 (2007/10/02)

Reaction of 21-alkyl ethers 1, 4-6, 8, a...

Regiospecific deoxygenation of the dihydroxyacetone moiety at C-17 of corticoid steroids with iodotrimethylsilane.

Numazawa,Nagaoka,Kunitama

, p. 3722 - 3726 (2007/10/02)

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72-23-1 Process route

Pregnenolone
145-13-1

Pregnenolone

Corticosterone
50-22-6

Corticosterone

11-dehydrocorticosterone
72-23-1

11-dehydrocorticosterone

19,21-dihydroxypregn-4-ene-3,20-dione
2394-23-2

19,21-dihydroxypregn-4-ene-3,20-dione

18,21-dihydroxy-4-pregnen-3,20-dione
10385-97-4

18,21-dihydroxy-4-pregnen-3,20-dione

Conditions
Conditions Yield
With air; dibutyric cyclic AMP; enucleated male Sprague-Dawley rat adrenal glands after feeding for 72 h with 1 percent NaCl; NaHCO3 buffer; at 37 ℃; for 3h; Product distribution; tritium labeled study;
Cortisone
53-06-5

Cortisone

11-Ketoprogesterone
516-15-4

11-Ketoprogesterone

11-dehydrocorticosterone
72-23-1

11-dehydrocorticosterone

Conditions
Conditions Yield
With trimethylsilyl iodide; In chloroform; for 3h; Ambient temperature;
10%
84%
With trimethylsilyl iodide; In chloroform; for 2h; Ambient temperature;
10%
84%
With trimethylsilyl iodide; In acetonitrile; for 3h; Ambient temperature;
27%
46%
With trimethylsilyl iodide; In acetonitrile; for 3h; Ambient temperature;
27%
46%

72-23-1 Upstream products

  • 516-15-4
    516-15-4

    11-Ketoprogesterone

  • 1173-27-9
    1173-27-9

    21-acetoxy-pregn-4-ene-3,11,20-trione

  • 39703-68-9
    39703-68-9

    rac -21-acetoxy-3,3-ethanediyldioxy-pregn-5-ene-11,20-dione

  • 53-06-5
    53-06-5

    Cortisone

72-23-1 Downstream products

  • 124113-69-5
    124113-69-5

    1-(3,11,20-trioxo-pregn-4-en-21-yl)-pyridinium; toluene-4-sulfonate

  • 116-56-3
    116-56-3

    11-dehydro-20-dihydrocorticosterone

  • 92010-58-7
    92010-58-7

    Δ4 -pregnen-21-ol-3,11,20-trione p-fluorobenzoate

  • 129786-20-5
    129786-20-5

    21-(Trityloxy)pregn-4-ene-3,11,20-trione

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