Welcome to LookChem.com Sign In|Join Free
  • or
3,11β,17α,21-tetraacetoxy-3,5-pregnadiene-20-one is a complex steroidal compound characterized by the presence of four acetoxy groups at the 3, 11β, 17α, and 21 positions, and a double bond between carbons 3 and 5 in the pregnadiene structure. This molecule features a 20-ketone functional group, indicating the presence of a carbonyl group at the 20th carbon position. It belongs to the class of steroids, which are a group of naturally occurring organic compounds that play a crucial role in various biological processes, including hormone regulation and cellular signaling. The specific arrangement of functional groups in 3,11β,17α,21-tetraacetoxy-3,5-pregnadiene-20-one may confer unique properties and potential applications in pharmaceutical or chemical research, although further context or details about its specific use or synthesis would be necessary to provide a more comprehensive understanding.

991-08-2

Post Buying Request

991-08-2 Suppliers

Recommended suppliers

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

991-08-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 991-08-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,9 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 991-08:
(5*9)+(4*9)+(3*1)+(2*0)+(1*8)=92
92 % 10 = 2
So 991-08-2 is a valid CAS Registry Number.

991-08-2Downstream Products

991-08-2Relevant academic research and scientific papers

Microwave induced selective enolization of steroidal ketones and efficient acetylation of sterols in semisolid state

Marwah, Padma,Marwah, Ashok,Lardy, Henry A.

, p. 2273 - 2287 (2003)

Under microwave irradiation steroidal enones, more specifically, position three carbonyls were efficiently and selectively converted to the corresponding enol acetates in the presence of additional enolizable carbonyl functions at other positions, using acetic anhydride and a catalytic amount of toluene-p-sulfonic acid. Acetylation of hydroxyl groups of the sterols, including those at the hindered positions, was near quantitative. Strictly anhydrous conditions were not a pre-requisite for acetylation and the reaction system easily tolerated up to 10% (v/v) moisture.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1 Customer Service

What can I do for you?
Get Best Price

Get Best Price for 991-08-2