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N-(4-morpholinyl-2-nitrophenyl)acetamide is a chemical compound with the molecular formula C10H12N4O4. It is an organic molecule that features a 2-nitrophenyl group attached to a morpholine ring, with an acetamide group connected to the nitrogen atom of the morpholine. N-(4-morpholinyl-2-nitrophenyl)acetamide is known for its potential applications in the pharmaceutical industry, particularly as a precursor in the synthesis of various drugs. Its structure allows for the exploration of different chemical reactions and modifications, making it a versatile building block in medicinal chemistry. The compound's properties, such as its reactivity and stability, are influenced by the presence of the nitro group, which can participate in reduction reactions, and the morpholine ring, which contributes to the compound's solubility and potential interactions with biological targets.

5367-49-7

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5367-49-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5367-49-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,3,6 and 7 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 5367-49:
(6*5)+(5*3)+(4*6)+(3*7)+(2*4)+(1*9)=107
107 % 10 = 7
So 5367-49-7 is a valid CAS Registry Number.

5367-49-7Downstream Products

5367-49-7Relevant academic research and scientific papers

Heterocycle type derivative and preparing method and pharmaceutical application thereof

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Paragraph 0243; 0246; 0251-0253, (2018/07/30)

The invention relates to a novel heterocycle type derivative, a preparing method thereof, a medicine composition containing the derivative and application of the heterocycle type derivative as therapeutic agent, particularly an FGFR4 inhibitor. The preferable compound has a good inhibiting effect on FGFR4.

Novel small molecules with selective cytotoxicity against human microvascular endothelial cell proliferation

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Page/Page column 21-22, (2010/11/28)

Disclosed herein are angiogenesis inhibitors represented by formula (I) or formula (II): The variables for formulas (I) and (II) are defined herein.

Synthesis of meta-substituted aniline derivatives by nucleophilic substitution

Belfield, Andrew J.,Brown, George R.,Foubister, Alan J.,Ratcliffe, Paul D.

, p. 13285 - 13300 (2007/10/03)

Substitution by amines of fluorobenzenes containing a meta- substituted electron withdrawing group (EWG), in DMSO at 100 °C over 60 h gave meta-substituted aniline derivatives in isolated yields of up to 98%. The scope of the reaction is explored in terms of reaction conditions and substrates. It is postulated that facile meta-substitutions are facilitated through field stabilisation of the intermediate anion by EWG substituents.

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