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CAS

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71455-90-8

methyl N-[N-(p-chlorobenzoyl)-4-(p-anisidino)butyryl]-4-(p-anisidino)butyrate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 71455-90-8 Structure

  • Basic information

    1. Product Name: methyl N-[N-(p-chlorobenzoyl)-4-(p-anisidino)butyryl]-4-(p-anisidino)butyrate
    2. Synonyms:
    3. CAS NO:71455-90-8
    4. Molecular Formula:
    5. Molecular Weight: 553.055
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 71455-90-8.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: methyl N-[N-(p-chlorobenzoyl)-4-(p-anisidino)butyryl]-4-(p-anisidino)butyrate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl N-[N-(p-chlorobenzoyl)-4-(p-anisidino)butyryl]-4-(p-anisidino)butyrate(71455-90-8)
    11. EPA Substance Registry System: methyl N-[N-(p-chlorobenzoyl)-4-(p-anisidino)butyryl]-4-(p-anisidino)butyrate(71455-90-8)

  • 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: 71455-90-8(Hazardous Substances Data)

71455-90-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 71455-90-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,4,5 and 5 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71455-90:
(7*7)+(6*1)+(5*4)+(4*5)+(3*5)+(2*9)+(1*0)=128
128 % 10 = 8
So 71455-90-8 is a valid CAS Registry Number.

71455-90-8Downstream Products

71455-90-8Relevant articles and documents

N-(Substituted amino)alkanoyl-aminoalkanoic acids and salts, their use and their compositions

-

, (2008/06/13)

N-substituted ω-aminoalkanoyl-ω-aminoalkanoic acids and their pharmacologically-acceptable salts (with a base) are useful, e.g., in pharmaceutical-composition form for the treatment or prophylaxis of diseases which are based on inadequate performance of the pancreas, the bile and/or the liver. The compounds are prepared, e.g., by reacting an N-(mono- or di-substituted) ω-amino-alkanoic acid with an N-(unsubstituted or monosubstituted) ω-aminoalkanoic acid.

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