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CAS

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25883-01-6

Benzoic acid, 3-(acetylmethylamino)-5-[(3-carboxy-1-oxopropyl)amino]-2,4,6-triiodo- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 25883-01-6 Structure

  • Basic information

    1. Product Name: Benzoic acid, 3-(acetylmethylamino)-5-[(3-carboxy-1-oxopropyl)amino]-2,4,6-triiodo-
    2. Synonyms:
    3. CAS NO:25883-01-6
    4. Molecular Formula: C14H13I3N2O6
    5. Molecular Weight: 685.981
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 25883-01-6.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: Benzoic acid, 3-(acetylmethylamino)-5-[(3-carboxy-1-oxopropyl)amino]-2,4,6-triiodo-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzoic acid, 3-(acetylmethylamino)-5-[(3-carboxy-1-oxopropyl)amino]-2,4,6-triiodo-(25883-01-6)
    11. EPA Substance Registry System: Benzoic acid, 3-(acetylmethylamino)-5-[(3-carboxy-1-oxopropyl)amino]-2,4,6-triiodo-(25883-01-6)

  • 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: 25883-01-6(Hazardous Substances Data)

25883-01-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25883-01-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,8,8 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 25883-01:
(7*2)+(6*5)+(5*8)+(4*8)+(3*3)+(2*0)+(1*1)=126
126 % 10 = 6
So 25883-01-6 is a valid CAS Registry Number.

25883-01-6Downstream Products

25883-01-6Relevant articles and documents

Iodinated anilic acids

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, (2008/06/13)

3-Amino-2,4,6-triiodobenzoic acids optionally substituted in the 5-position by amino or carboxy or a derivative thereof react with dibasic acid anhydrides to give the corresponding cyclic imides (A), which can be hydrolyzed to the corresponding anilic aci

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