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2-Nitrophenyl pentyl ether, with the chemical formula C12H17NO3, is an organic compound characterized by the attachment of a nitrophenyl group to a pentyl ether group. This yellowish solid is known for its low solubility in water and is recognized for its potential hazards, including flammability and the capacity to cause skin and eye irritation.

39645-91-5

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39645-91-5 Usage

Uses

Used in Pharmaceutical Synthesis:
2-Nitrophenyl pentyl ether is utilized as a key intermediate in the synthesis of various pharmaceuticals, contributing to the development of new drugs and therapeutic agents.
Used in Agrochemical Production:
In the agrochemical industry, 2-Nitrophenyl pentyl ether serves as a crucial component in the production of pesticides and other crop protection agents, enhancing agricultural productivity and crop protection.
Used in Fragrance Industry:
2-Nitrophenyl pentyl ether is employed as a raw material in the creation of fragrances, adding unique scents to a variety of consumer products, including perfumes, cosmetics, and household items.
Used as an Industrial Solvent:
2-NITROPHENYL PENTYL ETHER is also used as a solvent in several industrial applications, facilitating processes that require the dissolution of specific substances or materials for manufacturing purposes.

Check Digit Verification of cas no

The CAS Registry Mumber 39645-91-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,6,4 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 39645-91:
(7*3)+(6*9)+(5*6)+(4*4)+(3*5)+(2*9)+(1*1)=155
155 % 10 = 5
So 39645-91-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H15NO3/c1-2-3-6-9-15-11-8-5-4-7-10(11)12(13)14/h4-5,7-8H,2-3,6,9H2,1H3

39645-91-5 Well-known Company Product Price

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  • Sigma-Aldrich

  • (73741)  2-Nitrophenylpentylether  Selectophore, ≥99.0%

  • 39645-91-5

  • 73741-5ML

  • 857.61CNY

  • Detail

39645-91-5Relevant academic research and scientific papers

Boron-Promoted Ether Interchange Reaction: Synthesis of Alkyl Nitroaromatic Ethers from Methoxynitroarenes

Liu, Zhenwei,Luan, Nannan,Lu, Hongtao,Liang, Apeng,Li, Jingya,Zou, Dapeng,Wu, Yangjie,Wu, Yusheng

, p. 702 - 707 (2020/02/11)

The first protocol for boron-promoted ether interchange reaction of methoxynitroarenes was described. A series of methoxynitroarenes and alcohols, including primary, secondary, as well as tertiary alcohols were reacted smoothly in moderate to good yields under the optimized reaction conditions. This protocol constitutes an operationally simple and scalable strategy for the synthesis of alkyl nitroaromatic ethers. Moreover, the new reactivity of boron reagents was discovered.

Investigations on the 4-quinolone-3-carboxylic acid motif. 4. Identification of new potent and selective ligands for the cannabinoid type 2 receptor with diverse substitution patterns and antihyperalgesic effects in mice

Pasquini, Serena,De Rosa, Maria,Pedani, Valentina,Mugnaini, Claudia,Guida, Francesca,Luongo, Livio,De Chiaro, Maria,Maione, Sabatino,Dragoni, Stefania,Frosini, Maria,Ligresti, Alessia,Di Marzo, Vincenzo,Corelli, Federico

supporting information; experimental part, p. 5444 - 5453 (2011/09/30)

Experimental evidence suggests that selective CB2 receptor modulators may provide access to antihyperalgesic agents devoid of psychotropic effects. Taking advantage of previous findings on structure-activity/selectivity relationships for a class of 4-quin

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