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2-IODO-4-(1-METHYLETHYL)BENZENAMINE is a chemical compound with the molecular formula C10H14IN, characterized as a substituted aniline derivative. It has a molecular weight of 271.13 g/mol and presents as a pale yellow powder. 2-IODO-4-(1-METHYLETHYL)BENZENAMINE is insoluble in water but soluble in organic solvents such as ethanol and ether. Its chemical structure, which includes both iodo and alkyl groups, makes it a versatile building block for the synthesis of various organic molecules. It is primarily recognized for its role as an intermediate in the synthesis of pharmaceuticals and other organic compounds, and it also holds potential in the research and development of novel pharmaceuticals and agrochemicals. However, due to its potential hazards and reactivity, careful handling is required.

76842-15-4

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76842-15-4 Usage

Uses

Used in Pharmaceutical Industry:
2-IODO-4-(1-METHYLETHYL)BENZENAMINE is used as a chemical intermediate for the synthesis of various pharmaceuticals, contributing to the development of new medications and therapeutic agents.
Used in Organic Synthesis:
It serves as a versatile building block in organic synthesis, enabling the creation of a wide range of organic compounds for different applications.
Used in Research and Development:
2-IODO-4-(1-METHYLETHYL)BENZENAMINE is utilized in research and development for the exploration and creation of novel pharmaceuticals and agrochemicals, expanding the horizons of chemical and medical innovation.
Used in Agrochemical Industry:
It is also employed as an intermediate in the synthesis of agrochemicals, playing a role in the development of new products for agricultural applications.

Check Digit Verification of cas no

The CAS Registry Mumber 76842-15-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,8,4 and 2 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 76842-15:
(7*7)+(6*6)+(5*8)+(4*4)+(3*2)+(2*1)+(1*5)=154
154 % 10 = 4
So 76842-15-4 is a valid CAS Registry Number.

76842-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-iodo-4-isopropylaniline

1.2 Other means of identification

Product number -
Other names 2-iodo-isopropylaniline

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:76842-15-4 SDS

76842-15-4Upstream product

76842-15-4Relevant academic research and scientific papers

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

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Paragraph 0269-0272, (2021/06/09)

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

New indolo[1,2-c]quinazolines for single-crystal field-effect transistor: A united experimental and theoretical studies

Puli, Venkat Swamy,Kilaru, Suresh,Bhongiri, Yadagiri,Marri, Sreenath Reddy,Tripathi, Anuj,Chetti, Prabhakar,Chatterjee, Anindita,Vukoti, Kiran Kumar,Pola, Someshwar

, (2021/08/30)

Here, we account the synthesis and characterization of a series of symmetrical fused heterocyclic aromatic hydrocarbons (HAHs) with an indolo[1,2-c]quinazoline (IQ) as the core moiety. All the new HAHs IQ series were systematically investigated by using various spectroscopic methods. Furthermore, their photo-physical properties were supported by density functional theory (DFT) and time-dependent density functional theory (TDDFT) studies to support the experimental findings. The tetramethyl-substituted indolo[1,2-c]quinazoline (TMIQ) compound is shown to exhibit the shifted type of π–π stacking interactions, which render this series as a new semiconducting material. Single-crystal-based field-effect transistor devices of TMIQ exhibited efficient charge transport behavior, giving a p-channel field-effect mobility of 0.25 cm2?V?1?s?1 with an on/off ratio of 5 × 105.

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

Rakshit, Amitava,Dhara, Hirendra Nath,Alam, Tipu,Dahiya, Anjali,Patel, Bhisma K.

supporting information, p. 17504 - 17510 (2021/11/18)

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.

Dispirofluorene-indenofluorene (DSFIF): Synthesis, electrochemical, and optical properties of a promising new family of luminescent materials

Horhant, David,Liang, Jing-Jing,Virboul, Morgane,Poriel, Cyril,Alcaraz, Gilles,Rault-Berthelot, Joelle

, p. 257 - 260 (2007/10/03)

A series of new dispiro[fluorene-9′,6,9″,12-indeno[1,2b] fluorenes] (DSFIFs) that combine indenofluorene (IF) and spirobifluorene (SBF) architectural specificities have been prepared. Their anodic oxidations lead to the formation of nonsoluble transparent

AROMATIC AMIDES

-

, (2008/06/13)

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.

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