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[2-(3-Fluoro-4-methoxy-phenyl)-1H-indol-3-ylmethyl]-dimethyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 77445-38-6 Structure
  • Basic information

    1. Product Name: [2-(3-Fluoro-4-methoxy-phenyl)-1H-indol-3-ylmethyl]-dimethyl-amine
    2. Synonyms: [2-(3-Fluoro-4-methoxy-phenyl)-1H-indol-3-ylmethyl]-dimethyl-amine
    3. CAS NO:77445-38-6
    4. Molecular Formula:
    5. Molecular Weight: 298.36
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 77445-38-6.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: [2-(3-Fluoro-4-methoxy-phenyl)-1H-indol-3-ylmethyl]-dimethyl-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: [2-(3-Fluoro-4-methoxy-phenyl)-1H-indol-3-ylmethyl]-dimethyl-amine(77445-38-6)
    11. EPA Substance Registry System: [2-(3-Fluoro-4-methoxy-phenyl)-1H-indol-3-ylmethyl]-dimethyl-amine(77445-38-6)
  • 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: 77445-38-6(Hazardous Substances Data)

77445-38-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77445-38-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,4,4 and 5 respectively; the second part has 2 digits, 3 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 77445-38:
(7*7)+(6*7)+(5*4)+(4*4)+(3*5)+(2*3)+(1*8)=156
156 % 10 = 6
So 77445-38-6 is a valid CAS Registry Number.

77445-38-6Downstream Products

77445-38-6Relevant articles and documents

I2-induced cascade cyclization and dearomatization of indoles for the highly efficient synthesis of iodinated and vinylic spiroindolenines

Li, Yazhou,Liang, Xuewu,Liu, Hong,Liu, Qi,Liu, Xuyi,Wei, Xiaohui,Zhou, Yu

supporting information, p. 9165 - 9171 (2021/11/23)

The spiroindolenine framework is a privileged heterocyclic motif and is widely present in numerous indole alkaloids. Herein, we develop a metal-free and environmentally friendly approach for the intramolecular cascade cyclization and dearomatization of indole derivatives to selectively afford iodinated and vinylic spiroindolenines by a substrate-controlled strategy. Simple operation, mild conditions, and high yield make this strategy a green and attractive pathway to construct functionalizable spiroindolenine scaffolds, which could be converted into diverse useful spiroindolenine derivatives.

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