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9-(4-methylbenzylidene)-9H-xanthene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 68066-89-7 Structure
  • Basic information

    1. Product Name: 9-(4-methylbenzylidene)-9H-xanthene
    2. Synonyms: 9-(4-methylbenzylidene)-9H-xanthene
    3. CAS NO:68066-89-7
    4. Molecular Formula:
    5. Molecular Weight: 284.357
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 68066-89-7.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: 9-(4-methylbenzylidene)-9H-xanthene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 9-(4-methylbenzylidene)-9H-xanthene(68066-89-7)
    11. EPA Substance Registry System: 9-(4-methylbenzylidene)-9H-xanthene(68066-89-7)
  • 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: 68066-89-7(Hazardous Substances Data)

68066-89-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 68066-89-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,0,6 and 6 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 68066-89:
(7*6)+(6*8)+(5*0)+(4*6)+(3*6)+(2*8)+(1*9)=157
157 % 10 = 7
So 68066-89-7 is a valid CAS Registry Number.

68066-89-7Downstream Products

68066-89-7Relevant articles and documents

Pd-Catalyzed Autotandem Reactions with N-Tosylhydrazones. Synthesis of Condensed Carbo- and Heterocycles by Formation of a C-C Single Bond and a C-C Double Bond on the Same Carbon Atom

Paraja, Miguel,Valdés, Carlos

, p. 2034 - 2037 (2017/04/27)

A new Pd-catalyzed autotandem reaction is introduced that consists of the cross-coupling of a benzyl bromide with a N-tosylhydrazone followed by an intramolecular Heck reaction with an aryl bromide. During the process, a single and a double C-C bond are formed on the same carbon atom. Two different arrangements for the reactive functional groups are possible, rendering great flexibility to the transformation. The same strategy led to 9-methylene-9H-fluorenes, 9-methylene-9H-xanthenes, 9-methylene-9,10-dihydroacridines, and also dihydropyrroloisoquinoline and dihydroindoloisoquinoline derivatives.

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