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326595-65-7

7-BROMO-2,4-DIMETHYL-1H-INDOLE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 326595-65-7 Structure

  • Basic information

    1. Product Name: 7-BROMO-2,4-DIMETHYL-1H-INDOLE
    2. Synonyms: 7-BROMO-2,4-DIMETHYL-1H-INDOLE
    3. CAS NO:326595-65-7
    4. Molecular Formula: C10H10BrN
    5. Molecular Weight: 224.1
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 326595-65-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    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: 7-BROMO-2,4-DIMETHYL-1H-INDOLE(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7-BROMO-2,4-DIMETHYL-1H-INDOLE(326595-65-7)
    11. EPA Substance Registry System: 7-BROMO-2,4-DIMETHYL-1H-INDOLE(326595-65-7)

  • 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: 326595-65-7(Hazardous Substances Data)

326595-65-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 326595-65-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,6,5,9 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 326595-65:
(8*3)+(7*2)+(6*6)+(5*5)+(4*9)+(3*5)+(2*6)+(1*5)=167
167 % 10 = 7
So 326595-65-7 is a valid CAS Registry Number.

326595-65-7Downstream Products

326595-65-7Relevant articles and documents

A Biomass-Derived Non-Noble Cobalt Catalyst for Selective Hydrodehalogenation of Alkyl and (Hetero)Aryl Halides

Sahoo, Basudev,Surkus, Annette-Enrica,Pohl, Marga-Martina,Radnik, J?rg,Schneider, Matthias,Bachmann, Stephan,Scalone, Michelangelo,Junge, Kathrin,Beller, Matthias

supporting information, p. 11242 - 11247 (2017/09/02)

Hydrodehalogenation is a straightforward approach for detoxifications of harmful anthropogenic organohalide-based pollutants, as well as removal of halide protecting groups used in multistep syntheses. A novel sustainable catalytic material was prepared from biowaste (chitosan) in combination with an earth-abundant cobalt salt. The heterogeneous catalyst was fully characterized by transmission electron microscope, X-ray diffraction, and X-ray photoelectron spectroscopy measurements, and successfully applied to hydrodehalogenation of alkyl and (hetero)aryl halides with broad scope (>40 examples) and excellent chemoselectivity using molecular hydrogen as a reductant. The general usefulness of this method is demonstrated by successful detoxification of non-degradable pesticides and fire retardants. Moreover, the potential of the catalyst as a deprotection tool is demonstrated in a multistep synthesis of (±)-peronatin B (alkaloid).

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