76842-15-4

Basic information

• Product Name: 2-IODO-4-(1-METHYLETHYL)BENZENAMINE
• Synonyms: 2-IODO-4-(1-METHYLETHYL)BENZENAMINE;2-IODO-4-ISOPROPYLANILINE;4-ISOPROPYL-2-IODOANILINE;2-iodo-4-isopropylbenzenamine
• CAS NO: 76842-15-4
• Molecular Formula: C₉H₁₂IN
• Molecular Weight: 261.11
• Mol File: 76842-15-4.mol
• Article Data: 5

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-IODO-4-(1-METHYLETHYL)BENZENAMINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-IODO-4-(1-METHYLETHYL)BENZENAMINE(76842-15-4)
• EPA Substance Registry System: 2-IODO-4-(1-METHYLETHYL)BENZENAMINE(76842-15-4)

Safety Data

• Hazardous Substances Data: 76842-15-4(Hazardous Substances Data)

Usage

General Description

2-IODO-4-(1-METHYLETHYL)BENZENAMINE is a chemical compound with the molecular formula C10H14IN. It is a substituted aniline derivative with a molecular weight of 271.13 g/mol. 2-IODO-4-(1-METHYLETHYL)BENZENAMINE is a pale yellow powder that is insoluble in water but soluble in organic solvents such as ethanol and ether. It is primarily used as an intermediate in the synthesis of pharmaceuticals and other organic compounds. Its chemical structure contains both iodo and alkyl groups, making it a versatile building block for the synthesis of various organic molecules. Additionally, it has potential applications in the research and development of novel pharmaceuticals and agrochemicals. However, it is important to handle this chemical with caution due to its potential hazards and reactivity.

Upstream product

• 99-88-7 4-Isopropylaniline 

Downstream Products

• 1415332-44-3 C₁₇H₁₇N 
• 1628347-67-0 2-{8-isopropyl-11-oxo-5H-dibenzo[b,e][1,4]diazepin-10(11H)-yl}benzonitrile 
• 1616975-08-6 5-isopropyl-1-tosylindolin-3-one 
• 1190199-91-7 2-ethynyl-4-(i-propyl)aniline 

Relevant articles and documents

Novel phenylcarbazole type organic compounds and an organic electroluminescent device comprising the same

An organic compound represented by chemical formula 1 and an organic light emitting device including the same are provided. Chemical Formula 1.

Cu(II)-Promoted Cascade Synthesis of Fused Imidazo-Pyridine-Carbonitriles

A Cu(II)-promoted synthesis of an aza-fused N-heterocycle having a benz-imidazopyridine scaffold is developed via an addition-cyclization reaction followed by an Ullmann-type C-N coupling between o-iodoanilines and γ-ketodinitriles. This protocol features a broad substrate scope, giving products in 32-84% yields. The compounds show excellent photoluminescence properties having two absorption maxima in the region between 270-280 and 338-350 nm and emission maxima in the range of 502-533 nm. The HOMO-LUMO energy gap of 3.49-3.57 eV was determined using Gaussian 09 at the B3LYP/6-31G (d, p) basis set level. We also demonstrated a few postsynthetic modifications.

AROMATIC AMIDES

This application relates to a compound of formula I (or a pharmaceutically acceptable salt thereof) as defined herein, pharmaceutical compositions thereof, and its use as an inhibitor of factor Xa, as well as a process for its preparation and intermediates therefor.