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6-Amino-5-(benzyloxy)-3-chlorobenzothiophen-2-carbonsaeure-methylester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

155587-75-0

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  • 155587-75-0 Structure

  • Basic information

    1. Product Name: 6-Amino-5-(benzyloxy)-3-chlorobenzothiophen-2-carbonsaeure-methylester
    2. Synonyms: 6-Amino-5-(benzyloxy)-3-chlorobenzothiophen-2-carbonsaeure-methylester
    3. CAS NO:155587-75-0
    4. Molecular Formula:
    5. Molecular Weight: 347.822
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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: 6-Amino-5-(benzyloxy)-3-chlorobenzothiophen-2-carbonsaeure-methylester(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-Amino-5-(benzyloxy)-3-chlorobenzothiophen-2-carbonsaeure-methylester(155587-75-0)
    11. EPA Substance Registry System: 6-Amino-5-(benzyloxy)-3-chlorobenzothiophen-2-carbonsaeure-methylester(155587-75-0)

  • 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: 155587-75-0(Hazardous Substances Data)

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155587-75-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 155587-75-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,5,8 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 155587-75:
(8*1)+(7*5)+(6*5)+(5*5)+(4*8)+(3*7)+(2*7)+(1*5)=170
170 % 10 = 0
So 155587-75-0 is a valid CAS Registry Number.

155587-75-0Relevant academic research and scientific papers

Synthesis and characterization of the furo and thieno analogues of the triester of PQQ

Martin,Winkler

, p. 100 - 110 (2007/10/02)

We report here the synthesis and properties of the furo and thieno analogues of 4,5-dihydro-4,5-dioxo-1H-pyrrolo[2,3-f]quinoline-2,7,9-tricarboxylic acid (=PQQ), i.e. the furo- and thieno[2,3-f]quinoline-4,5-quinone (FQQ and TQQ, resp.) derivatives B and C, obtained as triesters. The triester of PQQ derivative A is much more stable than the triesters of B or C, and only the triester of A shows strong activity in nonenzymatic catalytic oxidations.

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