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"Acetamide, N-(5-fluoro-4-methoxy-2-nitrophenyl)-" is a complex organic chemical compound with the molecular formula C9H8FN3O4. It is characterized by the presence of a fluorine atom at the 5th position, a methoxy group at the 4th position, and a nitro group at the 2nd position of the phenyl ring, which is attached to an acetamide group. Acetamide, N-(5-fluoro-4-methoxy-2-nitrophenyl)- is a derivative of acetamide, where the hydrogen atom of the amide group is replaced by a substituted phenyl ring. It is a yellow crystalline solid and is used in the synthesis of various pharmaceuticals and agrochemicals due to its unique chemical properties. The compound's structure and functional groups contribute to its reactivity and potential applications in chemical research and development.

448-26-0

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448-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 448-26-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,4 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 448-26:
(5*4)+(4*4)+(3*8)+(2*2)+(1*6)=70
70 % 10 = 0
So 448-26-0 is a valid CAS Registry Number.

448-26-0SDS

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 N-(5-fluoro-4-methoxy-2-nitrophenyl)acetamide

1.2 Other means of identification

Product number -
Other names acetic acid-(5-fluoro-4-methoxy-2-nitro-anilide)

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:448-26-0 SDS

448-26-0Relevant articles and documents

Benzimidazole compound, and preparation method, intermediate and application thereof

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, (2016/10/20)

The invention discloses a benzimidazole compound, and a preparation method, an intermediate and an application thereof. The invention provides a benzimidazole compound A or a pharmaceutically-acceptable salt thereof, and also provides an application of th

3,8-DIAZA-BICYCLO[4.2.0]OCT-3-YL AMIDES

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Page/Page column 80, (2012/07/13)

The present invention relates to 3,8-diaza-bicyclo[4.2.0]oct-3-yl amide derivatives of formula (I), wherein the relative configuration of the diazabicyclooctane moiety is cis; and wherein Ar1, and Ar2 are as described in the description, to their preparation, to pharmaceutically acceptable salts thereof, and to their use as pharmaceuticals, to pharmaceutical compositions containing one or more compounds of formula (I), and especially to their use as orexin receptor antagonists.

COUMARIN DERIVATIVE AND USE THEREOF

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Page/Page column 96, (2008/06/13)

The present invention relates to an alkaline earth metal salt or an organic amine salt of a compound represented by the formula [I]: wherein R1 and R2 are each a hydrogen atom, a halogen atom, or an optionally substituted linear hydrocarbon group; ring A is an optionally further substituted benzene ring; B is an optionally substituted benzene ring; R is a carboxyl group or a linear hydrocarbon group substituted with a carboxyl group and the like.

Positive allosteric modulators of the nicotinic acetylcholine receptor

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Page 44, (2010/02/05)

The invention provides compounds of Formula I: These compounds may be in the form of pharmaceutical salts or compositions, may be in pure enantiomeric form or racemic mixtures, and are useful in pharmaceuticals used to treat diseases or conditions in which α7 nAChR is known to be involved.

4-Methyl-5-(unsubstituted and substituted phenoxy)-6-methoxy-8-(aminoalkylamino)quinolines

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, (2008/06/13)

Compounds of the class including 4-methyl-5-(unsubstituted and substitutedhenoxy)-6-methoxy-8-(aminoalkylamino)quinolines as the free bases and pharmaceutically acceptable acid amine salts are described. The compounds are highly effective antimalarial agents which possess, surprisingly, both tissue schizonticidal (radical curative) and blood schizonticidal (suppressive) activity. In addition, these drugs have significantly better therapeutics indices than primaquine which is the current tissue schizonticidal drug of choice. Primaquine possesses no useful blood schizonticidal activity at tolerated dose levels.

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