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5-(4-Nitrophenyl)furfuryl alcohol is a chemical compound with the molecular formula C12H9NO4. It is a yellow crystalline solid that is often used as a versatile intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. This chemical is known for its nitro-substituted phenyl and furfuryl alcohol groups, which contribute to its unique reactivity and biological activity.

33342-30-2

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33342-30-2 Usage

Uses

Used in Pharmaceutical Industry:
5-(4-Nitrophenyl)furfuryl alcohol is used as a versatile intermediate for the synthesis of various pharmaceuticals due to its unique reactivity and biological activity.
Used in Agrochemical Industry:
5-(4-Nitrophenyl)furfuryl alcohol is used as a building block in the production of agrochemicals, contributing to the development of effective and innovative products.
Used in Organic Compounds Synthesis:
5-(4-Nitrophenyl)furfuryl alcohol is used as a key intermediate in the synthesis of various organic compounds, enabling the creation of a wide range of chemical products.
Used as a Flavor and Fragrance Ingredient:
5-(4-Nitrophenyl)furfuryl alcohol is used as a flavor and fragrance ingredient in various products, adding unique scents and tastes to consumer goods.
Used in Antimicrobial and Antifungal Applications:
5-(4-Nitrophenyl)furfuryl alcohol has been studied for its potential pharmacological properties, including its antimicrobial and antifungal activities, making it a promising candidate for use in healthcare and sanitation products.

Check Digit Verification of cas no

The CAS Registry Mumber 33342-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,3,4 and 2 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 33342-30:
(7*3)+(6*3)+(5*3)+(4*4)+(3*2)+(2*3)+(1*0)=82
82 % 10 = 2
So 33342-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C11H9NO4/c13-7-10-5-6-11(16-10)8-1-3-9(4-2-8)12(14)15/h1-6,13H,7H2

33342-30-2SDS

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 [5-(4-nitrophenyl)furan-2-yl]methanol

1.2 Other means of identification

Product number -
Other names 5-(4-nitrophenyl)-2-furylmethanol

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:33342-30-2 SDS

33342-30-2Relevant academic research and scientific papers

Synthesis of 2,5-Diaryl Nonsymmetric Furans C6-Platform Chemicals via Catalytic Conversion of Biomass and the Formal Synthesis of Dantrolene

Chacón-Huete, Franklin,Lasso, Juan David,Szavay, Paul,Covone, Jason,Forgione, Pat

, p. 515 - 524 (2020/12/22)

Biomass-derived commodity chemical 5-hydroxymethyl furfural is an underutilized C6-platform chemical derived from cellulose that is ideal to prepare next-generation value-added products. We have developed an efficient synthetic strategy to access 2,5-diar

Zinc phthalocyanine with PEG-400 as a recyclable catalytic system for selective reduction of aromatic nitro compounds

Sharma, Upendra,Kumar, Neeraj,Verma, Praveen Kumar,Kumar, Vishal,Singh, Bikram

supporting information; experimental part, p. 2289 - 2293 (2012/09/10)

Zinc phthalocyanine with PEG-400 was established as a catalytic system for chemo and regioselective reduction of aromatic nitro compounds to corresponding amines. A large range of reducible functional groups such as acid, amide, ester, halogen, lactone, nitrile, N-benzyl, O-benzyl, hydroxy and heterocycles were well tolerated. Direct synthesis of benzotriazole from O-dinitrobenzene was achieved for the first time. The present catalytic system was successfully employed for the reduction of carbonyl and ester compounds to corresponding alcohols and reductive amination of benzaldehydes with primary amines to form corresponding secondary amines. Remarkable advantages of the present catalytic method include low loading of metal, avoidance of toxic ligands and high isolated yields. The catalyst was recyclable up to four times without any loss of selectivity and activity.

Palladium-catalysed direct arylation of heteroaromatics bearing unprotected hydroxyalkyl functions using aryl bromides

Roger, Julien,Pozgan, Franc,Doucet, Henri

experimental part, p. 696 - 710 (2010/06/19)

Heteroaromatics bearing unprotected hydroxyalkyl functions can be arylated using aryl or heteroaryl bromides, via palladium-catalysed carbonhydrogen bond activation/arylation. Good yields were generally obtained using 0.01-0.5 mol% of the air-stable palladium acetate complex as the catalyst. The nature of the base was found to be crucial for the selectivity of this reaction. Potassium acetate led to the direct arylation products whereas caesium car-bonate led to the formation of the ether. This procedure is certainly more atom-economic than other methods for the preparation of such compounds, as no protection/ deprotection sequence of the hydroxyalkyl function and no preparation of an organometallic derivative is required.

5-(4-Nitrophenyl)-2-furanmethanamines derivatives

-

, (2008/06/13)

Certain 5-(4-nitrophenyl)-2-furanmethanamines are useful as anthelmintic agents.

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