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(E)-N-methyl-N-(3-phenyl-2-propenyl)-3-benzofuranmethanamine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

98977-77-6

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  • 98977-77-6 Structure
  • Basic information

    1. Product Name: (E)-N-methyl-N-(3-phenyl-2-propenyl)-3-benzofuranmethanamine
    2. Synonyms: (E)-N-methyl-N-(3-phenyl-2-propenyl)-3-benzofuranmethanamine
    3. CAS NO:98977-77-6
    4. Molecular Formula:
    5. Molecular Weight: 277.366
    6. EINECS: N/A
    7. Product Categories: N/A
  • 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: (E)-N-methyl-N-(3-phenyl-2-propenyl)-3-benzofuranmethanamine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-N-methyl-N-(3-phenyl-2-propenyl)-3-benzofuranmethanamine(98977-77-6)
    11. EPA Substance Registry System: (E)-N-methyl-N-(3-phenyl-2-propenyl)-3-benzofuranmethanamine(98977-77-6)
  • 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: 98977-77-6(Hazardous Substances Data)

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98977-77-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 98977-77-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,9,7 and 7 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 98977-77:
(7*9)+(6*8)+(5*9)+(4*7)+(3*7)+(2*7)+(1*7)=226
226 % 10 = 6
So 98977-77-6 is a valid CAS Registry Number.

98977-77-6Downstream Products

98977-77-6Relevant academic research and scientific papers

BENZOHETEROCYCLYL ALKYLAMINE COMPOUND AND USE THEREOF

-

, (2019/10/16)

Disclosed are benzoheterocyclic alkylamine compounds, or a pharmaceutically acceptable salt thereof, or a stereoisomer thereof, and a preparation method thereof, and use of the same in the manufacture of an antibacterial drug as an inhibitor of staphyloxanthin synthesis in Staphylococcus aureus.

Synthesis and Structure-Activity Relationships of Naftifine-Related Allylamine Antimycotics

Stuetz, Anton,Georgopoulos, Apostolos,Granitzer, Waltraud,Petranyi, Gabor,Berney, Daniel

, p. 112 - 125 (2007/10/02)

Naftifine (1) is the first representative of the new antifungal allylamine derivatives.Its biological activity is strictly bound to specific structural requirements that are unrelated to those of known antifungals.A tertiary allylamine function seems to be a prerequisite for activity against fungi.By systematic variation of the individual structural elements in 1, detailed structure-activity relationships are defined in which the phenyl ring is the structural feature permitting the widest variations.Versatile synthetic routes to allylamine derivatives and comparative biological data are presented.

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