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17903-99-0

4-Acetoxy-3-(acetylamino)benzoic acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 17903-99-0 Structure

  • Basic information

    1. Product Name: 4-Acetoxy-3-(acetylamino)benzoic acid
    2. Synonyms:
    3. CAS NO:17903-99-0
    4. Molecular Formula:
    5. Molecular Weight: 237.212
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17903-99-0.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-Acetoxy-3-(acetylamino)benzoic acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-Acetoxy-3-(acetylamino)benzoic acid(17903-99-0)
    11. EPA Substance Registry System: 4-Acetoxy-3-(acetylamino)benzoic acid(17903-99-0)

  • 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: 17903-99-0(Hazardous Substances Data)

17903-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17903-99-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,9,0 and 3 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 17903-99:
(7*1)+(6*7)+(5*9)+(4*0)+(3*3)+(2*9)+(1*9)=130
130 % 10 = 0
So 17903-99-0 is a valid CAS Registry Number.

17903-99-0Relevant articles and documents

Aromatic sialic acid analogues as potential inhibitors of influenza virus neuraminidase

Bianco, Armandodoriano,Brufani, Mario,Melchioni, Cristiana

, p. 305 - 309 (2007/10/03)

The influenza virus neuraminidase (NA) is an enzyme essential for viral infection and offers a potential target for antiviral drug development. We aimed our research at the synthesis of non-carbohydrate molecules able to inhibit NA as transition-state ana

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