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91902-18-0

Acetamide, N-[2-[(3-nitro-2-pyridinyl)thio]phenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 91902-18-0 Structure

  • Basic information

    1. Product Name: Acetamide, N-[2-[(3-nitro-2-pyridinyl)thio]phenyl]-
    2. Synonyms:
    3. CAS NO:91902-18-0
    4. Molecular Formula: C13H11N3O3S
    5. Molecular Weight: 289.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 91902-18-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Acetamide, N-[2-[(3-nitro-2-pyridinyl)thio]phenyl]-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Acetamide, N-[2-[(3-nitro-2-pyridinyl)thio]phenyl]-(91902-18-0)
    11. EPA Substance Registry System: Acetamide, N-[2-[(3-nitro-2-pyridinyl)thio]phenyl]-(91902-18-0)

  • 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: 91902-18-0(Hazardous Substances Data)

91902-18-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91902-18-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,9,0 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 91902-18:
(7*9)+(6*1)+(5*9)+(4*0)+(3*2)+(2*1)+(1*8)=130
130 % 10 = 0
So 91902-18-0 is a valid CAS Registry Number.

91902-18-0SDS

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-[2-(3-nitropyridin-2-yl)sulfanylphenyl]acetamide

1.2 Other means of identification

Product number -
Other names 2-acetylaminophenyl-(3-nitro-2-pyridyl)sulfide

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:91902-18-0 SDS

91902-18-0Relevant articles and documents

COMPOUND, ORGANIC LiGHT EMITTING DIODE INCLUDING THE SAME, COMPOSITION INCLUDING THE SAME AND DISPLAY INCLUDING THE ORGANIC LiGHT EMITTING DIODE

-

, (2016/10/09)

The present invention relates to a compound, an organic light emitting diode including the same, a composition for the organic light emitting diode including the same, and a display device comprising the organic light emitting diode. The present invention is to provide a compound which can provide an organic photoelectron diode having high efficiency and long service life. To this end, provided is a compound for an organic photoelectron diode represented by chemical formula 1.

Synthesis and antimicrobial activity of novel bis-azaphenothiazines

Kushwaha, Khushbu,Sakhuja, Rajeev,Jain, Subhash C.

, p. 4459 - 4467 (2013/09/02)

N-alkylation of azaphenothiazines using dibromoalkanes or dibromoalkenes did not result in the formation of bis-azaphenothiazines under known conditions such as refluxing, for more than 100 h, with NaNH2/xylene or NaH/toluene. However, when the same reaction was tried with NaH/DMF at -5 C to r.t., it yielded the desired product in 68-71 % yield. These novel bis-azaphenothiazines containing a suitable alkyl or alkenyl spacer were found to possess moderate to significant antimicrobial activities against three gram positive bacteria (Staphylococcus aureus, Bacillus subtilis, and Staphylococcus epidermis), four gram negative bacteria (Escherichia coli, Pseudomonas aeruginosa, Salmonella typhi, and Klebsiella pneumoniae) as well as four fungi (Aspergillus niger, Aspergillus fumigatus, Aspergillus flavus, and Candida albicans). Compounds 2b-d were found to exhibit strong antifungal activity, comparable to the standard drug miconazole against A. niger and A. fumigatus.

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