Welcome to LookChem.com Sign In|Join Free
  • or
4-fluoro-N-(4-iodophenyl)benzamide is a chemical compound with the molecular formula C13H9FIINO. It is a derivative of benzamide, featuring a 4-fluoro substituent on the benzene ring and a 4-iodophenyl group attached to the nitrogen atom. 4-fluoro-N-(4-iodophenyl)benzamide is known for its potential applications in the field of pharmaceuticals and medicinal chemistry, particularly as a building block for the synthesis of more complex molecules with therapeutic properties. Its structure allows for the exploration of structure-activity relationships in drug design, as the presence of halogenated substituents can significantly influence the pharmacokinetics and pharmacodynamics of a molecule. The compound is also of interest due to its potential role in the development of new drugs targeting various diseases, including cancer and neurological disorders.

326-03-4

Post Buying Request

326-03-4 Suppliers

Recommended suppliers

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

326-03-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 326-03-4 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,2 and 6 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 326-03:
(5*3)+(4*2)+(3*6)+(2*0)+(1*3)=44
44 % 10 = 4
So 326-03-4 is a valid CAS Registry Number.

326-03-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-fluoro-N-(4-iodophenyl)-benzamide

1.2 Other means of identification

Product number -
Other names 4-Fluoro-N-(4-iodophenyl)benzamide

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:326-03-4 SDS

326-03-4Relevant academic research and scientific papers

Role of Hetero-halogen (F · · · X, X = Cl, Br, and I) or homo-halogen (X · · · X, X = F, Cl, Br, and I) interactions in substituted benzanilides

Nayak, Susanta K.,Kishore Reddy,Row, Tayur N. Guru,Chopra, Deepak

experimental part, p. 1578 - 1596 (2012/04/04)

A series of halogen-substituted benzanilides have been synthesized and characterized, and crystallization studies directed toward generation of polymorphs have been performed to delineate the importance of interactions involving halogens. The effect of ha

Synthesis of pharmacologically relevant indoles with amine side chains via tandem hydroformylation/fischer indole synthesis

Schmidt, Axel M.,Eilbracht, Peter

, p. 5528 - 5535 (2007/10/03)

The sequence of hydroformylation and Fischer indole synthesis starting from amino olefins and aryl hydrazines is described. In a convergent manner, the two units bearing pharmacologically relevant substituents are assembled in the final indolization step. This modular and diversity-oriented approach to tryptamines and homotryptamines can be conducted in water and allows synthesis of branched and nonbranched tryptamines as well as tryptamine-based pharmaceuticals such as the 5-HT1D agonist L 775 606.

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 326-03-4