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CAS

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1313809-59-4

6-bromo-1-methoxy-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1313809-59-4 Structure

  • Basic information

    1. Product Name: 6-bromo-1-methoxy-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole
    2. Synonyms: 6-bromo-1-methoxy-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole
    3. CAS NO:1313809-59-4
    4. Molecular Formula:
    5. Molecular Weight: 400.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1313809-59-4.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: 6-bromo-1-methoxy-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-bromo-1-methoxy-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole(1313809-59-4)
    11. EPA Substance Registry System: 6-bromo-1-methoxy-9-(4-methoxybenzyl)-1,2,3,4-tetrahydro-9H-carbazole(1313809-59-4)

  • 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: 1313809-59-4(Hazardous Substances Data)

1313809-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1313809-59-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,8,0 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1313809-59:
(9*1)+(8*3)+(7*1)+(6*3)+(5*8)+(4*0)+(3*9)+(2*5)+(1*9)=144
144 % 10 = 4
So 1313809-59-4 is a valid CAS Registry Number.

1313809-59-4Downstream Products

1313809-59-4Relevant articles and documents

Sulfoxide-TFAA and nucleophile combination as new reagent for aliphatic C-H functionalization at indole 2α-position

Tayu, Masanori,Higuchi, Kazuhiro,Inaba, Masato,Kawasaki, Tomomi

supporting information, p. 496 - 502 (2013/02/23)

Aliphatic C-H functionalization at indole 2α-position mediated by acyloxythionium species 1 generated from sulfoxide and acid anhydride has been developed. The combination of sulfoxide and TFAA with O-, N- and C-nucleophiles enabled introduction of various substituents in a one-pot procedure. Especially on utilizing DMSO, the combination provided a practical and efficient method for the synthesis of a wide range of 2α-substituted indoles. The Royal Society of Chemistry 2013.

Active thionium species mediated functionalization at the 2α-position of indole derivatives

Higuchi, Kazuhiro,Tayu, Masanori,Kawasaki, Tomomi

, p. 6728 - 6730 (2011/07/07)

A combination of dimethyl sulfoxide (DMSO) and trifluoroacetic anhydride (TFAA) mediates functionalization at the 2α-position of indole derivatives. Carbon and heteroatom nucleophiles were directly introduced via a one-pot procedure in excellent yields.

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