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2,3,10bβ,11,12,12aβ-Hexahydro-1α,2β,4aβ,8-tetrahydroxy-11,11-dimethyl-2,12α-methano-1H-benzo[b]naphtho[2,1-d]pyran-4(4aH)-one

  • Name 2,3,10bβ,11,12,12aβ-Hexahydro-1α,2β,4aβ,8-tetrahydroxy-11,11-dimethyl-2,12α-methano-1H-benzo[b]naphtho[2,1-d]pyran-4(4aH)-one
  • CAS 2618-41-9
  • Purity 99%
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Product Details

Cost-effective and customizable 2,3,10bβ,11,12,12aβ-Hexahydro-1α,2β,4aβ,8-tetrahydroxy-11,11-dimethyl-2,12α-methano-1H-benzo[b]naphtho[2,1-d]pyran-4(4aH)-one 2618-41-9 factory

  • Molecular Formula: C20H22 O6
  • Molecular Weight: 358.391
  • Vapor Pressure: 1.73E-14mmHg at 25°C 
  • Melting Point: 270 °C 
  • Boiling Point: 584.1°Cat760mmHg 
  • PKA: 9.46±0.70(Predicted) 
  • Flash Point: 211.7°C 
  • PSA: 107.22000 
  • Density: 1.54g/cm3 
  • LogP: 1.22390 

2,3,10bβ,11,12,12aβ-Hexahydro-1α,2β,4aβ,8-tetrahydroxy-11,11-dimethyl-2,12α-methano-1H-benzo[b]naphtho[2,1-d]pyran-4(4aH)-one(Cas 2618-41-9) Usage

InChI:InChI=1/C20H22O6/c1-18(2)11-6-19(24)7-14(22)20(25,16(11)17(19)23)12-8-26-13-5-9(21)3-4-10(13)15(12)18/h3-5,8,11,15-17,21,23-25H,6-7H2,1-2H3/t11-,15+,16-,17+,19+,20-/m0/s1

2618-41-9 Relevant articles

Enantioselective total synthesis of miroestrol

Corey,Wu

, p. 9327 - 9328 (2007/10/02)

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2618-41-9 Process route

C<sub>38</sub>H<sub>62</sub>O<sub>6</sub>Si<sub>2</sub>

C38 H62 O6 Si2

miroestrol
2618-41-9

miroestrol

Conditions
Conditions Yield
With tetrabutyl ammonium fluoride; In tetrahydrofuran; at 0 ℃; for 0.0833333h;
94%
C<sub>38</sub>H<sub>62</sub>O<sub>5</sub>Si<sub>2</sub>

C38 H62 O5 Si2

miroestrol
2618-41-9

miroestrol

Conditions
Conditions Yield
Multi-step reaction with 3 steps
1: 90 percent / Et3 N / CH2 Cl2 / 18 h / Heating
2: 63 percent / SeO2 , t-BuOOH / CH2 Cl2 / 60 h
3: 94 percent / n-Bu4 NF / tetrahydrofuran / 0.08 h / 0 °C
With tert.-butylhydroperoxide; selenium(IV) oxide; tetrabutyl ammonium fluoride; triethylamine; In tetrahydrofuran; dichloromethane;
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