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109543-48-8

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

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  • 109543-48-8 Structure

  • Basic information

    1. Product Name: 3-amino-4-quinolinethiol
    2. Synonyms: 3-amino-4-quinolinethiol;3-Amino-4-mercaptoquinoline
    3. CAS NO:109543-48-8
    4. Molecular Formula: C9H8N2S
    5. Molecular Weight: 176.23822
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 109543-48-8.mol

  • Chemical Properties

    1. Melting Point: 190℃
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-amino-4-quinolinethiol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-amino-4-quinolinethiol(109543-48-8)
    11. EPA Substance Registry System: 3-amino-4-quinolinethiol(109543-48-8)

  • 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: 109543-48-8(Hazardous Substances Data)

109543-48-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 109543-48-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,5,4 and 3 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 109543-48:
(8*1)+(7*0)+(6*9)+(5*5)+(4*4)+(3*3)+(2*4)+(1*8)=128
128 % 10 = 8
So 109543-48-8 is a valid CAS Registry Number.

109543-48-8Relevant articles and documents

Convenient synthesis of 2-aminonaphthalene-1-thiol and 3-aminoquinoline-4-thiol and cyclocondensations to 1,4-thiazino and 1,4-thiazepino derivatives

Ambrogi,Grandolini,Perioli,Rossi

, p. 656 - 658 (2007/10/02)

An improved method for the synthesis of 2-aminonaphthalene-1-thiol and an alternative procedure for the preparation of 3-aminoquinoline-4-thiol are described. From these intermediates some 1,4-thiazino and 1,4-thiazepino tricyclic derivatives have been prepared.

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