Welcome to LookChem.com Sign In|Join Free
  • or
N-(3-(2-bromophenyl)propyl)acetamide, commonly known as Flutamide, is an antiandrogen medication that functions by inhibiting the effects of androgen hormones in the body. This chemical compound is primarily utilized in the medical treatment of prostate cancer and hirsutism, playing a crucial role in managing the growth and spread of cancer cells as well as alleviating symptoms related to excessive hair growth.

178809-21-7

Post Buying Request

178809-21-7 Suppliers

Recommended suppliers

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

178809-21-7 Usage

Uses

Used in Pharmaceutical Industry:
Flutamide is used as an antiandrogen medication for the treatment of prostate cancer, a condition where the growth and spread of cancer cells are influenced by androgen hormones. By blocking these hormones, Flutamide helps to slow down the progression of the disease and improve the patient's quality of life.
Additionally, Flutamide is used as a therapeutic agent for hirsutism, a medical condition characterized by excessive hair growth in women. The medication works by reducing the effects of androgen hormones, which are responsible for this abnormal hair growth, thereby helping to manage and alleviate the symptoms.

Check Digit Verification of cas no

The CAS Registry Mumber 178809-21-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,8,8,0 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 178809-21:
(8*1)+(7*7)+(6*8)+(5*8)+(4*0)+(3*9)+(2*2)+(1*1)=177
177 % 10 = 7
So 178809-21-7 is a valid CAS Registry Number.

178809-21-7Relevant academic research and scientific papers

Radical C(sp3)-H alkenylation, alkynylation and allylation of ethers and amides enabled by photocatalysis

Paul, Subhasis,Guin, Joyram

supporting information, p. 2530 - 2534 (2017/07/17)

An efficient radical addition/elimination reaction that enables selective incorporation of alkenyl, alkynyl and allyl functional groups into the C(sp3)-H bond under green reaction conditions is developed. The process is based on the catalytic formation of α-alkoxyl/α-amidyl radicals via the homolytic activation of the C(sp3)-H bond of ethers/amides with a catalytic amount of diarylketone in the presence of a household fluorescent light bulb. This simple reaction protocol features good functional group tolerance, scalability, convenient reagents and operating systems. Synthetic application of the method has been demonstrated via the preparation of natural products and different valuable synthones.

RENIN INHIBITORS

-

Page/Page column 29, (2009/04/25)

The present invention relates to biphenyl compounds of formula (I). These compounds are renin inhibitors of a non- peptidic nature and of low molecular weight. The invention further relates to a pharmaceutical composition containing said compounds, as wel

Intramolecular palladium-catalyzed aryl amination and aryl amidation

Wolfe, John P.,Rennels, Roger A.,Buchwald, Stephen L.

, p. 7525 - 7546 (2007/10/03)

Upon treatment with a palladium catalyst and a suitable base, aromatic halides undergo intramolecular substitution to form five, six, and seven-membered rings. In a similar fashion aryl halides with pendant amides or sulfonamides are cyclized to form five and six-membered rings.

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 178809-21-7