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  • 127473-28-3 Structure
  • Basic information

    1. Product Name: 1H-Indol-5-ol, 1-methyl-2,3-diphenyl-
    2. Synonyms:
    3. CAS NO:127473-28-3
    4. Molecular Formula: C21H17NO
    5. Molecular Weight: 299.372
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127473-28-3.mol
    9. Article Data: 1
  • 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: 1H-Indol-5-ol, 1-methyl-2,3-diphenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Indol-5-ol, 1-methyl-2,3-diphenyl-(127473-28-3)
    11. EPA Substance Registry System: 1H-Indol-5-ol, 1-methyl-2,3-diphenyl-(127473-28-3)
  • 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: 127473-28-3(Hazardous Substances Data)

127473-28-3 Usage

Class

Indoles (heterocyclic compounds with a six-membered ring and two nitrogen atoms)

Derivative

1-methyl-2,3-diphenyl-1H-indol-5-ol

Usage

Chemical and pharmaceutical applications (valuable building block for the synthesis of other organic compounds)

Potential

Biological activities (subject of ongoing research in medicinal chemistry and drug development)

Check Digit Verification of cas no

The CAS Registry Mumber 127473-28-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,4,7 and 3 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 127473-28:
(8*1)+(7*2)+(6*7)+(5*4)+(4*7)+(3*3)+(2*2)+(1*8)=133
133 % 10 = 3
So 127473-28-3 is a valid CAS Registry Number.

127473-28-3Relevant articles and documents

Glycosylation of 2,3-Diphenylindole and Derivatives - Synthesis of O-, N-, and C-Glycopyranosides

El-Desoky, El-Sayed I.,Abdel-Rahman, Hassan A. R.,Schmidt, Richard R.

, p. 877 - 881 (2007/10/02)

Reaction of different glycosyl donors with 5-hydroxy-N-methyl-2,3-diphenylindole (1C) led only to O-glycosylation compounds 6a - c and 8c-α,β).Depending on the O-protection of the glycosyl donors (2a - c, 3b, 4c), the β-products were obtained mainly or e

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