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328045-73-4

2-(broMoMethyl)-1-Methyl-1H-indole-3-carbonitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 328045-73-4 Structure

  • Basic information

    1. Product Name: 2-(broMoMethyl)-1-Methyl-1H-indole-3-carbonitrile
    2. Synonyms: 2-(broMoMethyl)-1-Methyl-1H-indole-3-carbonitrile
    3. CAS NO:328045-73-4
    4. Molecular Formula: C11H9BrN2
    5. Molecular Weight: 249.10656
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 328045-73-4.mol

  • Chemical Properties

    1. Melting Point: 159.0-160.3 °C
    2. Boiling Point: 392.0±27.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.44±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 2-(broMoMethyl)-1-Methyl-1H-indole-3-carbonitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(broMoMethyl)-1-Methyl-1H-indole-3-carbonitrile(328045-73-4)
    11. EPA Substance Registry System: 2-(broMoMethyl)-1-Methyl-1H-indole-3-carbonitrile(328045-73-4)

  • 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: 328045-73-4(Hazardous Substances Data)

328045-73-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 328045-73-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,8,0,4 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 328045-73:
(8*3)+(7*2)+(6*8)+(5*0)+(4*4)+(3*5)+(2*7)+(1*3)=134
134 % 10 = 4
So 328045-73-4 is a valid CAS Registry Number.

328045-73-4Relevant articles and documents

Copper-catalyzed benzylic C-H oxygenation under an oxygen atmosphere via N-H imines as an intramolecular directing group

Zhang, Line,Ang, Gim Yean,Chiba, Shunsuke

supporting information; experimental part, p. 1622 - 1625 (2011/05/05)

Copper-catalyzed benzylic C-H oxygenation under an oxygen atmosphere was developed starting from carbonitriles and Grignard reagents via N-H imine intermediates. The present process is characterized by the following two-step sequence in a one-pot manner: (1) addition of Grignard reagents to carbonitriles to form N-H imines and (2) benzylic C-H oxygenation (C=O bond formation) triggered by 1,5-hydrogen atom transfer with transient iminyl copper species.

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