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N-(4-nitro-1,2-dihydroacenaphthylen-5-yl)acetamide is a complex organic chemical compound with the molecular formula C16H13N3O3. It is derived from the acenaphthene family, which consists of fused polycyclic aromatic hydrocarbons. This specific compound features a nitro group at the 4-position and an acetamide group attached to the 5-position of the acenaphthene core. The presence of the nitro group imparts potential reactivity and the ability to undergo reduction reactions, while the acetamide group provides amine-like properties. N-(4-nitro-1,2-dihydroacenaphthylen-5-yl)acetamide may be of interest in the fields of organic synthesis, medicinal chemistry, and materials science, where its unique structure could offer specific chemical or physical properties.

4889-61-6

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4889-61-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4889-61-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 4889-61:
(6*4)+(5*8)+(4*8)+(3*9)+(2*6)+(1*1)=136
136 % 10 = 6
So 4889-61-6 is a valid CAS Registry Number.

4889-61-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(4-nitro-1,2-dihydroacenaphthylen-5-yl)acetamide

1.2 Other means of identification

Product number -
Other names 4-Nitro-5-acetamino-acenaphthen

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 -
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More Details:4889-61-6 SDS

4889-61-6Relevant academic research and scientific papers

Sterically Congested Polycyclic Hydrocarbons with Nonoptimal Geometries. 4,5-Didehydroacenaphthene as a Precursor for the Synthesis of 7,14-Diphenyl-8,9-(1',8'-naphthenylene)acephenanthrene

Plummer, Benjamin F.,Russell, Steven J.,Reese, W. Gregory,Watson, William H.,Krawiec, Mariusz

, p. 3219 - 3223 (2007/10/02)

A multistep synthetic route for the synthesis of the reactive intermediate 4,5-didehydroacenaphthene (15) is described.A mixture of N-1-, N-2-, and N-3-aminoacenaphthotriazoles is produced, which is oxidized by lead tetraacetate (LTA) to the corresponding aryne.The N-2-triazole is oxidized by LTA to 7-cyano-1-(cyanomethylene)indan (18), whose structure was verified by X-ray analysis.Intermediate 15 was trapped by 7,9-diphenyl-8H-cyclopentaacenaphthylen-8-one (acecyclone) to produce the congested hydrocarbon 7,14-diphenyl-8,9-(1',8'-naphthenylene)acephenanthrene (20).There is a small deviation from planarity for 20, and this is modeled by MMX calculations and verified by X-ray crystallographic analysis of the structure.

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