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180194-87-0

4-amino-3-phenoxypyridine-N-oxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 180194-87-0 Structure

  • Basic information

    1. Product Name: 4-amino-3-phenoxypyridine-N-oxide
    2. Synonyms: 4-amino-3-phenoxypyridine-N-oxide
    3. CAS NO:180194-87-0
    4. Molecular Formula:
    5. Molecular Weight: 202.213
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 180194-87-0.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: 4-amino-3-phenoxypyridine-N-oxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-amino-3-phenoxypyridine-N-oxide(180194-87-0)
    11. EPA Substance Registry System: 4-amino-3-phenoxypyridine-N-oxide(180194-87-0)

  • 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: 180194-87-0(Hazardous Substances Data)

180194-87-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 180194-87-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,0,1,9 and 4 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 180194-87:
(8*1)+(7*8)+(6*0)+(5*1)+(4*9)+(3*4)+(2*8)+(1*7)=140
140 % 10 = 0
So 180194-87-0 is a valid CAS Registry Number.

180194-87-0Downstream Products

180194-87-0Relevant articles and documents

Synthesis and pharmacological evaluation of derivatives structuraily related to nimesulide

Cignarella,Vianello,Berti,Rossoni

, p. 359 - 364 (1996)

The present work reports the synthesis of a series of compounds structurally related to the antiinflammatory and antihistaminic agent nimesulide (I), in which the p-nitrophenyl moiety has been replaced by pyridine (1a-c) and pyridine N-oxide (2a-c). In addition, two compounds (3a, 4a) have been synthesized in which the p-nitro group of I was substituted by a cyano and a 1H-tetrazol-5-yl group, respectively. Representative 1a and 2a were also modified by replacing the methanesulfonamido group with an acetamido group (5a, 6a). The pharmacological evaluation of compounds 1-6 in comparison to I, indicates that such modifications are detrimental to the activity. Moreover 3a and 4a caused bronchoconstriction and hypotension, thus behaving as histaminic-like rather then antihistaminic agents.

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