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6716-65-0

1-(4-methoxycarbonylphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole is a complex organic compound with a molecular formula of C18H20N2O2. It is a derivative of the pyridoindole class, which is characterized by a fused pyridine and indole ring system. This specific compound features a 4-methoxycarbonylphenyl group attached to the pyridoindole core, which contributes to its unique chemical properties. The compound is of interest in the field of medicinal chemistry due to its potential applications as a precursor in the synthesis of various bioactive molecules, such as pharmaceuticals and agrochemicals. Its structure and properties make it a valuable candidate for further research and development in the creation of new therapeutic agents.

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  • 6716-65-0 Structure

  • Basic information

    1. Product Name: 1-(4-methoxycarbonylphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole
    2. Synonyms: 1-(4-methoxycarbonylphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole
    3. CAS NO:6716-65-0
    4. Molecular Formula:
    5. Molecular Weight: 306.364
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 6716-65-0.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: 1-(4-methoxycarbonylphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(4-methoxycarbonylphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole(6716-65-0)
    11. EPA Substance Registry System: 1-(4-methoxycarbonylphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole(6716-65-0)

  • 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: 6716-65-0(Hazardous Substances Data)

6716-65-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6716-65-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,7,1 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6716-65:
(6*6)+(5*7)+(4*1)+(3*6)+(2*6)+(1*5)=110
110 % 10 = 0
So 6716-65-0 is a valid CAS Registry Number.

6716-65-0Relevant articles and documents

Design, synthesis and biological evaluations of quaternization harman analogues as potential antibacterial agents

Dai, Jiangkun,Dan, Wenjia,Ren, Siyu,Shang, Congguo,Wang, Junru

, p. 23 - 36 (2018)

Thirty-three new quaternization harman analogues were synthesized and their antibacterial activity against four Gram-positive and two Gram-negative bacteria were evaluated. The structure–activity relationships were summarized and compounds 4f, 4i, 4l, 4u,

COMPOUNDS AND METHOD OF USE

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Paragraph 1075, (2019/09/06)

This present disclosure relates to compounds with ferroptosis inducing activity, a method of treating a subject with cancer with the compounds, and combination treatments with a second therapeutic agent.

METHOD OF SCREENING FOR AGENTS FOR DIFFERENTIATING STEM CELLS

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Paragraph 0477-0478, (2018/11/02)

The present application discloses a method for identifying an agent for the treatment or prevention of cancer or metastatic cancer comprising the steps of contacting stem cell with a potential agent, and identifying an agent that induces differentiation, or inhibits stem cell pluripotency or growth of the stem cell, wherein such agent is determined to be an anti-cancer agent.

AGENTS FOR DIFFERENTIATING STEM CELLS AND TREATING CANCER

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Paragraph 00554-00555, (2018/10/25)

The present application discloses a method for identifying an agent for the treatment or prevention of cancer or metastatic cancer comprising the steps of contacting stem cell with a potential agent, and identifying an agent that induces differentiation, or inhibits stem cell pluripotency or growth of the stem cell, wherein such agent is determined to be an anti-cancer agent.

A mild and efficient route to 2-benzyl tryptamine derivatives via ring-opening of β-carbolines

Hadjaz, Fariza,Yous, Sa?d,Lebegue, Nicolas,Berthelot, Pascal,Carato, Pascal

experimental part, p. 10004 - 10008 (2009/04/03)

We described a mild and easy method, in two steps, by which various benzyl groups were introduced in the C-2 position of tryptamine. The first step consisted on the synthesis of β-carbolines, starting from tryptamine derivatives, by a Pictet-Spengler reaction. Ring-opening of the β-carbolines, by hydrogenation, led to the desired 2-substituted benzyl tryptamine indole products. A supplementary step of alkylation could be realized to give N-alkyl-2-substituted benzyl tryptamine. During these reactions, nitrogen atoms require no step of protection.

Antibacterial compounds

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, (2008/06/13)

Compounds of the formula (I) are disclosed and are useful in the treatment bacterial infections: wherein: R1 is Ar or Het; R2 is C1-6alkyl, (R″)2N-(CH2)m— or Ar—C0-6alkyl; X is H

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