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3-((3,4,5-trimethoxybenzylidene)amino)phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 387842-23-1 Structure
  • Basic information

    1. Product Name: 3-((3,4,5-trimethoxybenzylidene)amino)phenol
    2. Synonyms: 3-((3,4,5-trimethoxybenzylidene)amino)phenol
    3. CAS NO:387842-23-1
    4. Molecular Formula:
    5. Molecular Weight: 287.315
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 387842-23-1.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: 3-((3,4,5-trimethoxybenzylidene)amino)phenol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-((3,4,5-trimethoxybenzylidene)amino)phenol(387842-23-1)
    11. EPA Substance Registry System: 3-((3,4,5-trimethoxybenzylidene)amino)phenol(387842-23-1)
  • 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: 387842-23-1(Hazardous Substances Data)

387842-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 387842-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,7,8,4 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 387842-23:
(8*3)+(7*8)+(6*7)+(5*8)+(4*4)+(3*2)+(2*2)+(1*3)=191
191 % 10 = 1
So 387842-23-1 is a valid CAS Registry Number.

387842-23-1Downstream Products

387842-23-1Relevant articles and documents

Mechanistic investigation and implications of a sacrificial aniline for the tandem cascade synthesis of 4-aza-podophyllotoxin analogues

Jeedimalla, Nagalakshmi,Johns, Jennifer,Roche, Stéphane P.

, p. 5845 - 5848 (2013)

Mechanistic investigations were pursued to determine a plausible mechanism in the cascade reaction involving tetronic acid with aldehydes and anilines to generate the 4-aza-2,3-dehydropodophyllotoxin core structure. The mechanistic driven hypothesis paved

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