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4-(4-Fluoro-2-nitrophenyl)morpholine is a chemical compound with the molecular formula C11H12FNO3. It is a morpholine derivative that features a 4-fluoro-2-nitrophenyl group attached to the morpholine ring. 4-(4-Fluoro-2-nitrophenyl)morpholine is known for its unique reactivity and properties due to the presence of the nitro and fluoro groups, making it a valuable building block in organic synthesis.

238418-75-2

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238418-75-2 Usage

Uses

Used in Pharmaceutical Synthesis:
4-(4-Fluoro-2-nitrophenyl)morpholine is used as an intermediate in the synthesis of pharmaceutical drugs. Its unique structure and reactivity contribute to the development of new therapeutic agents.
Used in Agrochemical Production:
4-(4-Fluoro-2-nitrophenyl)morpholine is also utilized as an intermediate in the production of agrochemicals, where it can be incorporated into the synthesis of various pesticides and other agricultural chemicals to enhance their efficacy.
Used in Anti-Cancer Applications:
4-(4-Fluoro-2-nitrophenyl)morpholine has been studied for its potential use in anti-cancer applications. Its specific chemical properties may contribute to the development of new cancer treatments, although further research is needed to fully understand its potential in this area.
Used in Anti-Inflammatory Applications:
Additionally, 4-(4-Fluoro-2-nitrophenyl)morpholine has been investigated for its potential role in anti-inflammatory applications, suggesting that it could be a component in the development of new medications to treat inflammation-related conditions.
Used in Chemical Research and Development:
4-(4-Fluoro-2-nitrophenyl)morpholine is also used as a reagent in chemical research and development. Its unique properties make it a useful tool for exploring new chemical reactions and syntheses in the laboratory.

Check Digit Verification of cas no

The CAS Registry Mumber 238418-75-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,3,8,4,1 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 238418-75:
(8*2)+(7*3)+(6*8)+(5*4)+(4*1)+(3*8)+(2*7)+(1*5)=152
152 % 10 = 2
So 238418-75-2 is a valid CAS Registry Number.

238418-75-2 Well-known Company Product Price

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  • (Code)Product description
  • CAS number
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  • Alfa Aesar

  • (H63247)  4-(4-Fluoro-2-nitrophenyl)morpholine, 97%   

  • 238418-75-2

  • 1g

  • 235.0CNY

  • Detail
  • Alfa Aesar

  • (H63247)  4-(4-Fluoro-2-nitrophenyl)morpholine, 97%   

  • 238418-75-2

  • 5g

  • 882.0CNY

  • Detail
  • Alfa Aesar

  • (H63247)  4-(4-Fluoro-2-nitrophenyl)morpholine, 97%   

  • 238418-75-2

  • 25g

  • 3528.0CNY

  • Detail

238418-75-2SDS

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 4-(4-Fluoro-2-nitrophenyl)morpholine

1.2 Other means of identification

Product number -
Other names 5-fluoro-2-morpholinonitrobenzene

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:238418-75-2 SDS

238418-75-2Downstream Products

238418-75-2Relevant academic research and scientific papers

Decarboxylative ipso Amination of Activated Benzoic Acids

Pichette Drapeau, Martin,Bahri, Janet,Lichte, Dominik,Goo?en, Lukas J.

supporting information, p. 892 - 896 (2019/01/04)

In the presence of a bimetallic Pd/Cu system with 1,10-phenanthroline as the ligand and either air or N-methylmorpholine N-oxide as the oxidant, electron-deficient benzoic acids undergo oxidative decarboxylative coupling with unprotected amines. This operationally simple aniline synthesis is widely applicable with respect to the amine and gives good yields, even on multigram scale. The orthogonality of this reaction to other Pd-catalyzed cross-couplings allows the concise synthesis of multisubstituted arenes by sequential C?C, C?Cl, and C?N functionalizations. Mechanistic investigations suggest the intermediacy of a hypervalent Pd species.

DIKETOPIPERAZINE DERIVATIVES AS P2X7 MODULATORS

-

Page/Page column 83, (2010/11/17)

The invention provides a compound of formula (I) or a pharmaceutically acceptable salt thereof: (I) wherein: A represents an aryl, heteroaryl or heterocyclyl group; and any ring or ring system of said aryl or heteroaryl is optionally substituted with 1 to 3 substituents, which may be the same or different, selected from the group consisting of halogen, C1-6 alkyl, -CF3, - OCF3, cyano, C1-6 alkoxy, -NR10R11, -X-aryl, -X-heteroaryl and -X-heterocyclyl; R1, R2, R3, R4 and R5 independently represent hydrogen, fluorine, chlorine, -CF3, cyano or C1-6 alkyl, such that at least one of R1, R2, R3, R4 and R5 is other than hydrogen; R6, R7, R8, R9, R10 and R11 independently represent hydrogen or C1-6 alkyl; X represents a linker selected from a bond, -(CH2)n- and -O-(CH2)n-; and n represents an integer from 1 to 3. The compounds or salts modulate P2X7 receptor function and are capable of antagonizing the effects of ATP at the P2X7 receptor ("P2X7 receptor antagonists").

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