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7,7',7'',7'''-tetraacetoxy-3,4':6',6'':4'',3'''-tetraindolyl is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 127560-99-0 Structure
  • Basic information

    1. Product Name: 7,7',7'',7'''-tetraacetoxy-3,4':6',6'':4'',3'''-tetraindolyl
    2. Synonyms: 7,7',7'',7'''-tetraacetoxy-3,4':6',6'':4'',3'''-tetraindolyl
    3. CAS NO:127560-99-0
    4. Molecular Formula:
    5. Molecular Weight: 694.7
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 127560-99-0.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: 7,7',7'',7'''-tetraacetoxy-3,4':6',6'':4'',3'''-tetraindolyl(CAS DataBase Reference)
    10. NIST Chemistry Reference: 7,7',7'',7'''-tetraacetoxy-3,4':6',6'':4'',3'''-tetraindolyl(127560-99-0)
    11. EPA Substance Registry System: 7,7',7'',7'''-tetraacetoxy-3,4':6',6'':4'',3'''-tetraindolyl(127560-99-0)
  • 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: 127560-99-0(Hazardous Substances Data)

127560-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 127560-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,5,6 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 127560-99:
(8*1)+(7*2)+(6*7)+(5*5)+(4*6)+(3*0)+(2*9)+(1*9)=140
140 % 10 = 0
So 127560-99-0 is a valid CAS Registry Number.

127560-99-0Downstream Products

127560-99-0Relevant articles and documents

OXIDATION OF 4-, 6- AND 7-HYDROXYINDOLES.

Napolitano, Alessandra,d'Ischia, Marco,Prota, Giuseppe,Schultz, Thomas M.,Wolfram, Leszek J.

, p. 6749 - 6760 (2007/10/02)

Oxidation of 4-, 6- and 7-hydroxyindoles with sodium periodate in phosphate buffer at pH 7.0 leads to complex mixtures of oligomeric products, the majority of which have been isolated and characterised as the O-acetyl derivatives. 7-Hydroxyindole (6) gives predominantly the dimers 9 and 10 as well as the trimer 11 and the tetramer 12 in smaller amounts.The 4- and 6-hydroxy isomers 7 and 8 follow less clear-cut reaction paths, characterised by the formation of the oligomers 13-16 and 17-19 respectively, along with polymeric materials.The observed mode of polymerisation of hydroxyindoles 6-8 is apparently consistent with a mechanism involving nucleophilic addition of the starting indoles to the electrophilic positions of transient quinonimine or phenoxonium-like intermediates.

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