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1-[3-(4-methylphenoxy)prop-1-en-1-yl]-3-nitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

94299-09-9

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94299-09-9 Usage

Chemical structure

1-[3-(4-methylphenoxy)prop-1-en-1-yl]-3-nitrobenzene is an organic compound with a complex chemical structure consisting of a benzene ring, a nitro group, a prop-1-en-1-yl group, and a 3-(4-methylphenoxy) substituent.

Benzene ring

The core structure of the compound is a benzene ring, which is a six-membered carbon ring with alternating single and double bonds.

Nitro group

A nitro group (-NO2) is attached to the benzene ring, which is known for its reactivity and can influence the compound's properties.

Prop-1-en-1-yl group

A prop-1-en-1-yl group (-CH2-CH=CH2) is linked to the benzene ring, providing a carbon-carbon double bond that can participate in various chemical reactions.

3-(4-methylphenoxy) substituent

The prop-1-en-1-yl group is connected to the benzene ring through a 3-(4-methylphenoxy) substituent, which is a phenoxy group with a methyl group attached to the para position (the fourth carbon) of the phenyl ring.

Pharmaceutical and agrochemical synthesis

1-[3-(4-methylphenoxy)prop-1-en-1-yl]-3-nitrobenzene is often used as an intermediate in the synthesis of pharmaceuticals and agrochemicals due to its versatile chemical structure.

Potential hazards

1-[3-(4-methylphenoxy)prop-1-en-1-yl]-3-nitrobenzene should be handled with care due to its potential hazards, such as toxicity and flammability. Proper safety measures and precautions should be taken when working with this chemical.

Applications

The compound's complex structure and reactivity make it useful in the development of various pharmaceuticals and agrochemicals, contributing to its importance in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 94299-09-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,2,9 and 9 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 94299-09:
(7*9)+(6*4)+(5*2)+(4*9)+(3*9)+(2*0)+(1*9)=169
169 % 10 = 9
So 94299-09-9 is a valid CAS Registry Number.

94299-09-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(Z)-3-(4-methylphenoxy)prop-1-enyl]-3-nitrobenzene

1.2 Other means of identification

Product number -
Other names -

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:94299-09-9 SDS

94299-09-9Relevant academic research and scientific papers

Organic synthesis via magnetic attraction: Benign and sustainable protocols using magnetic nanoferrites

Nasir Baig,Varma, Rajender S.

, p. 398 - 417 (2013/03/14)

Magnetic nano-catalysts have been prepared using simple modification of iron ferrites. The nm size range of these particles facilitates the catalysis process, as an increased surface area is available for the reaction; the easy separation of the catalysts by an external magnet and their recovery and reuse are additional beneficial attributes. Glutathione bearing nano-ferrites have been used as organocatalysts for the Paal-Knorr reaction and homocoupling of boronic acids. Nanoferrites, post-synthetically modified by ligands, were used to immobilize nanometals (Cu, Pd, Ru, etc.) which enabled the development of efficient, sustainable and green procedures for azide-alkynes-cycloaddition (AAC) reactions, C-S coupling, O-allylation of phenol, Heck-type reactions and hydration of nitriles.

O-Allylation of phenols with allylic acetates in aqueous media using a magnetically separable catalytic system

Saha, Amit,Leazer, John,Varma, Rajender S.

supporting information; experimental part, p. 67 - 71 (2012/03/27)

Allylic ethers were synthesized in water using magnetically recoverable heterogeneous Pd catalyst via O-allylation of phenols with allylic acetates under ambient conditions. The aqueous reaction medium, easy recovery of the catasyst using an external magn

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