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CAS

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92959-73-4

Acetamide, N-[4-[2-(acetyloxy)ethyl]-2-nitrophenyl]is a complex organic compound that features an acetamide group and a nitrophenyl group connected by a 2-(acetyloxy)ethyl bridge. The presence of an acetate group and a nitro group indicates that Acetamide, N-[4-[2-(acetyloxy)ethyl]-2-nitrophenyl]- may exhibit reactivity and bioactivity, making it a candidate for various chemical and pharmaceutical applications. Its specific synthesis and formulation will determine its exact properties and uses, which could range from drug development to chemical research and manufacturing.

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  • 92959-73-4 Structure

  • Basic information

    1. Product Name: AcetaMide, N-[4-[2-(acetyloxy)ethyl]-2-nitrophenyl]-
    2. Synonyms: AcetaMide, N-[4-[2-(acetyloxy)ethyl]-2-nitrophenyl]-;N-[4-[2-(acetyloxy)ethyl]-2-nitrophenyl]Acetamide
    3. CAS NO:92959-73-4
    4. Molecular Formula: C12H14N2O5
    5. Molecular Weight: 266.24996
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92959-73-4.mol

  • Chemical Properties

    1. Melting Point: 77 °C(Solv: benzene (71-43-2); ligroine (8032-32-4))
    2. Boiling Point: 475.5±40.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.307±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 13.72±0.70(Predicted)
    10. CAS DataBase Reference: AcetaMide, N-[4-[2-(acetyloxy)ethyl]-2-nitrophenyl]-(CAS DataBase Reference)
    11. NIST Chemistry Reference: AcetaMide, N-[4-[2-(acetyloxy)ethyl]-2-nitrophenyl]-(92959-73-4)
    12. EPA Substance Registry System: AcetaMide, N-[4-[2-(acetyloxy)ethyl]-2-nitrophenyl]-(92959-73-4)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 92959-73-4(Hazardous Substances Data)

92959-73-4 Usage

Uses

Used in Pharmaceutical Applications:
Acetamide, N-[4-[2-(acetyloxy)ethyl]-2-nitrophenyl]is used as a pharmaceutical intermediate for the development of new drugs due to its potential reactivity and bioactivity, which can be harnessed to create novel therapeutic agents.
Used in Chemical Research:
In the field of chemical research, Acetamide, N-[4-[2-(acetyloxy)ethyl]-2-nitrophenyl]is utilized as a compound of interest for studying its unique properties and potential reactions, contributing to the advancement of chemical knowledge and innovation.
Used in Chemical Manufacturing:
Acetamide, N-[4-[2-(acetyloxy)ethyl]-2-nitrophenyl]may be employed in the chemical manufacturing industry as a component in the production of various chemical products, taking advantage of its complex structure and reactive groups.

Check Digit Verification of cas no

The CAS Registry Mumber 92959-73-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,9,5 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 92959-73:
(7*9)+(6*2)+(5*9)+(4*5)+(3*9)+(2*7)+(1*3)=184
184 % 10 = 4
So 92959-73-4 is a valid CAS Registry Number.

92959-73-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(4-acetamido-3-nitrophenyl)ethyl acetate

1.2 Other means of identification

Product number -
Other names -

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:92959-73-4 SDS

92959-73-4Relevant articles and documents

Interaction of polycationic Ni(II)-salophen complexes with G-quadruplex DNA

Lecarme, Laureline,Prado, Enora,De Rache, Aurore,Nicolau-Travers, Marie-Laure,Bonnet, Romaric,Heyden, Angeline Van Der,Philouze, Christian,Gomez, Dennis,Mergny, Jean-Louis,Jamet, Hlne,Defrancq, Eric,Jarjayes, Olivier,Thomas, Fabrice

, p. 12519 - 12531 (2015/01/16)

A series of nine Ni(II) salophen complexes involving one, two, or three alkyl-imidazolium side-chains was prepared. The lengths of the side-chains were varied from one to three carbons. The crystal structure of one complex revealed a square planar geometr

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