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CAS

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1425047-53-5

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

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  • 1425047-53-5 Structure

  • Basic information

    1. Product Name: 4-amino-N-isobutylbenzamidine hydrochloride
    2. Synonyms:
    3. CAS NO:1425047-53-5
    4. Molecular Formula:
    5. Molecular Weight: 227.737
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1425047-53-5.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-N-isobutylbenzamidine hydrochloride(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-amino-N-isobutylbenzamidine hydrochloride(1425047-53-5)
    11. EPA Substance Registry System: 4-amino-N-isobutylbenzamidine hydrochloride(1425047-53-5)

  • 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: 1425047-53-5(Hazardous Substances Data)

1425047-53-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1425047-53-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,5,0,4 and 7 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1425047-53:
(9*1)+(8*4)+(7*2)+(6*5)+(5*0)+(4*4)+(3*7)+(2*5)+(1*3)=135
135 % 10 = 5
So 1425047-53-5 is a valid CAS Registry Number.

1425047-53-5Downstream Products

1425047-53-5Relevant articles and documents

Synthesis, DNA interactions and anticancer evaluation of novel diamidine derivatives of 3,4-ethylenedioxythiophene

Stolic, Ivana,Avdicevic, Monika,Bregovic, Nikola,Piantanida, Ivo,Glavas-Obrovac, Ljubica,Bajic, Miroslav

, p. 457 - 467 (2013/06/05)

Eight novel diamidino 3,4-ethylenedioxythiophene-2,5-dicarboxanilides (5a-h), obtained by condensation reaction of 3,4-ethylenedioxythiophene-2,5- dicarbonyl chloride and corresponding 3- or 4-aminobenzamidines, were evaluated for interactions with double-stranded DNA and RNA, and their cytotoxicity was assayed against the panel of human cancer cell lines. All compounds preferentially bind into the minor groove of DNA and had higher affinity for DNA than for RNA. Compounds 5a-h showed a moderate antiproliferative effect toward the panel of seven carcinoma cells line, whereby the highest inhibitory potential was displayed by compound 5a with unsubstituted amidino moieties in para position.

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