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5-(2-Methyl-4-Nitrophenyl)-2-Furaldehyde is an organic compound that belongs to the class of aromatic homomono cyclic compounds. It is characterized by the presence of a methyl group and a nitro group attached to a phenyl ring, which is connected to a furan ring through an aldehyde group. The aldehyde, furan, and nitro groups, along with the phenyl ring, provide the chemically active and reactive centers of the molecule. The specific properties, such as solubility, melting and boiling points, and the exact uses of 5-(2-METHYL-4-NITROPHENYL)-2-FURALDEHYDE depend on the physical state and purity of the material. It is typically used in the production of other chemicals or as a research or laboratory reagent. Due to its potentially harmful effects, adequate care must be taken while handling this chemical.

329222-70-0

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329222-70-0 Usage

Uses

Used in Chemical Production:
5-(2-Methyl-4-Nitrophenyl)-2-Furaldehyde is used as an intermediate in the synthesis of various chemicals. Its chemically active groups make it a valuable component in the production of a wide range of compounds.
Used in Research and Laboratory Applications:
5-(2-Methyl-4-Nitrophenyl)-2-Furaldehyde is used as a research or laboratory reagent. Its unique structure and reactivity make it a useful tool for studying chemical reactions and processes in scientific research.

Check Digit Verification of cas no

The CAS Registry Mumber 329222-70-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,9,2,2 and 2 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 329222-70:
(8*3)+(7*2)+(6*9)+(5*2)+(4*2)+(3*2)+(2*7)+(1*0)=130
130 % 10 = 0
So 329222-70-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H9NO4/c1-8-6-9(13(15)16)2-4-11(8)12-5-3-10(7-14)17-12/h2-7H,1H3

329222-70-0SDS

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 5-(2-methyl-4-nitrophenyl)furan-2-carbaldehyde

1.2 Other means of identification

Product number -
Other names 2-Furancarboxaldehyde,5-(2-methyl-4-nitrophenyl)

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:329222-70-0 SDS

329222-70-0Relevant academic research and scientific papers

Preparation of novel phenylfuran-based cyanohydrin esters: Lipase-catalysed kinetic and dynamic resolution

Paizs, Csaba,Taehtinen, Petri,Lundell, Katri,Poppe, Laszlo,Irimie, Florin-Dan,Kanerva, Liisa T.

, p. 1895 - 1904 (2003)

A series of novel (R)-5-phenylfuran-2-yl cyanomethyl butanoates were prepared by Pseudomonas cepacia lipase-catalysed dynamic kinetic resolution in toluene. The method exploits a basic resin both for the racemization and formation of phenylfuran-based cyanohydrins and for the decomposition of acetone cyanohydrin in one-pot with enzymatic enantioselective acylation using vinyl butanoate. The lipase-catalysed methanolysis of racemic 5-phenylfuran-2-yl cyanomethyl butanoates in toluene with E ?100 was shown to be usable when the corresponding (S)-butanoates are needed. Candida antarctica lipase A provided racemic cyanohydrin butanoates with quantitative chemical yields under mild conditions.

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