Welcome to LookChem.com Sign In|Join Free
  • or
Zindoxifene, also known as ZD-1839, is a selective estrogen receptor modulator (SERM) that functions as an estrogen agonist in some tissues and an antagonist in others. It is primarily used in the treatment of breast cancer, particularly in postmenopausal women with hormone receptor-positive tumors. Zindoxifene works by binding to estrogen receptors, thereby blocking the effects of estrogen in breast cancer cells and inhibiting their growth. Additionally, it has been studied for its potential benefits in preventing osteoporosis and reducing the risk of cardiovascular diseases due to its agonistic effects on bone and lipid metabolism. However, it is not approved for these indications. The drug is taken orally and is generally well-tolerated, with side effects including hot flashes, nausea, and fatigue.

86111-26-4

Post Buying Request

86111-26-4 Suppliers

Recommended suppliers

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

86111-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 86111-26-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,6,1,1 and 1 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 86111-26:
(7*8)+(6*6)+(5*1)+(4*1)+(3*1)+(2*2)+(1*6)=114
114 % 10 = 4
So 86111-26-4 is a valid CAS Registry Number.
InChI:InChI=1/C21H21NO4/c1-5-22-20-11-10-18(26-15(4)24)12-19(20)13(2)21(22)16-6-8-17(9-7-16)25-14(3)23/h6-12H,5H2,1-4H3

86111-26-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(5-acetyloxy-1-ethyl-3-methylindol-2-yl)phenyl] acetate

1.2 Other means of identification

Product number -
Other names Zindoxifenum [Latin]

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:86111-26-4 SDS

86111-26-4Downstream Products

86111-26-4Relevant academic research and scientific papers

Modular counter-Fischer?indole synthesis through radical-enolate coupling

Chung, Hyunho,Kim, Jeongyun,Gonzalez-Montiel, Gisela A.,Cheong, Paul Ha-Yeon,Lee, Hong Geun

, p. 1096 - 1102 (2021/01/26)

A single-electron transfer mediated modular indole formation reaction from a 2-iodoaniline derivative and a ketone has been developed. This transition-metal-free reaction shows a broad substrate scope and unconventional regioselectivity trends. Moreover, important functional groups for further transformation are tolerated under the reaction conditions. Density functional theory studies reveal that the reaction proceeds by metal coordination, which converts a disfavored 5-endo-trig cyclization to an accessible 7-endo-trig process.

Rhodium(iii)-catalyzed indole synthesis at room temperature using the transient oxidizing directing group strategy

Shang, Yaping,Jonnada, Krishna,Yedage, Subhash Laxman,Tu, Hua,Zhang, Xiaofeng,Lou, Xin,Huang, Shijun,Su, Weiping

supporting information, p. 9547 - 9550 (2019/08/15)

Rh-catalyzed reactions of N-alkyl anilines with internal alkynes at room temperature have been developed using an in situ generated N-nitroso group as a transient oxidizing directing group. Due to mild reaction conditions, this method enabled synthesis of a broad range of N-alkyl indoles, including even two indole-based medicinal compounds. Our work disclosed the feasibility of the transient oxidizing directing group strategy in C-H functionalization reactions, which possesses the potential to enhance overall step-economy and impart new reactivity patterns to substrates.

2-Phenylindoles. Relationship between Structure, Estrogen Receptor Affinity, and Mammary Tumor Inhibiting Activity in the Rat

Angerer, Erwin von,Prekajac, Jelica,Strohmeier, Josef

, p. 1439 - 1447 (2007/10/02)

A number of 2-phenylindole derivatives with one hydroxy group in the meta or para position of the phenyl ring and a second one in position 5, 6, or 7 of the indole nucleus were synthesized.In addition, different alkyl groups were introduced into positions

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 86111-26-4