Welcome to LookChem.com Sign In|Join Free
  • or
(11beta,20S)-11,17,20-trihydroxy-3-oxopregna-1,4-dien-21-yl acetate is a steroid compound and a derivative of progesterone. It features a pregnane backbone with three hydroxyl groups at positions 11, 17, and 20, a ketone group at position 3, and an acetate group attached to the 21st carbon of the pregnane structure. (11beta,20S)-11,17,20-trihydroxy-3-oxopregna-1,4-dien-21-yl acetate plays a role in various biological processes in the human body, particularly in hormone regulation and signaling.
Used in Pharmaceutical Industry:
(11beta,20S)-11,17,20-trihydroxy-3-oxopregna-1,4-dien-21-yl acetate is used as a pharmaceutical agent for the development of medications targeting hormonal disorders and reproductive health. Its involvement in hormone regulation and signaling makes it a promising candidate for research and drug development in these areas.

2871-71-8

Post Buying Request

2871-71-8 Suppliers

Recommended suppliers

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

2871-71-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2871-71-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,8,7 and 1 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2871-71:
(6*2)+(5*8)+(4*7)+(3*1)+(2*7)+(1*1)=98
98 % 10 = 8
So 2871-71-8 is a valid CAS Registry Number.

2871-71-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 21-acetoxy-11Beta,17Alpha,20Alpha-trihydroxy 1,4-pregnadiene-3-one

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:2871-71-8 SDS

2871-71-8Upstream product

2871-71-8Relevant academic research and scientific papers

Reduction of steroidal ketones with amine - Boranes

Leontjev,Vasiljeva,Pivnitsky

, p. 703 - 708 (2007/10/03)

Complexes of secondary amines with borane, R2NH·BH 3, surpass sodium borohydride as reducing agents for saturated and unsaturated steroidal 3-, 12-, 17-, and 20-ketones as regards chemo- and regioselectivity and mildness of the reaction conditions. In the case of 12-ketones, stereoselectivity is also improved.

Anti-inflammatory carboxy pregnane derivatives

-

, (2008/06/13)

Compounds of the formula: STR1 wherein one X is COOR, CH2 COOR, CH(COOR)2, CONHR, CH2 CONHR, or CN remaining X's are H, F, CH3, OH, COOR, CH2 COOR, CH(COOR)2, CONHR, CH2 CONHR, or CN; Y is STR2 R is H, alkyl of 1-5 carbon atoms, or benzyl; R1 is CH2 OR3, COOR, or CONHR; R2 is H, OR3, or BR; R3 is H, COR4, or tetrahydropyranyl; R4 is alkyl of 1-5 carbon atoms or benzyl; R5 is H or COR4 ; represents a single or double bond; represents α-position, β-position, or a mixture of α- and β-positions; and --- represents α-position; and methods for preparing the same.

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 2871-71-8