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2,8-Decadien-1,10-diylidenbis(triphenylphosphoran) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 50376-06-2 Structure
  • Basic information

    1. Product Name: 2,8-Decadien-1,10-diylidenbis(triphenylphosphoran)
    2. Synonyms: 2,8-Decadien-1,10-diylidenbis(triphenylphosphoran)
    3. CAS NO:50376-06-2
    4. Molecular Formula:
    5. Molecular Weight: 658.803
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 50376-06-2.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: 2,8-Decadien-1,10-diylidenbis(triphenylphosphoran)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2,8-Decadien-1,10-diylidenbis(triphenylphosphoran)(50376-06-2)
    11. EPA Substance Registry System: 2,8-Decadien-1,10-diylidenbis(triphenylphosphoran)(50376-06-2)
  • 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: 50376-06-2(Hazardous Substances Data)

50376-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 50376-06-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,3,7 and 6 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 50376-06:
(7*5)+(6*0)+(5*3)+(4*7)+(3*6)+(2*0)+(1*6)=102
102 % 10 = 2
So 50376-06-2 is a valid CAS Registry Number.

50376-06-2Downstream Products

50376-06-2Relevant articles and documents

Open-chain and Cyclic Bis-phosphoranes from α,ω-Dinitriles, Diisobutylaluminium Hydride, and Methylenetriphenylphosphorane

Bogdanovic, Borislav,Hullen, Albert,Konstantinovic, Stanimir,Krawiecka, Bozena,Mynott, Richard

, p. 2261 - 2271 (2007/10/02)

The reaction of subero-, azelao-, and sebaconitrile (4, n = 6, 7, and 8) with diisobutylaluminium hydride (to give 5) and subsequenly with methylenetriphenylphosphorane leads to the openc-hain bis-phosphoranes 8 a-c, which have been characterized by the Wittig reaction.The same reaction sequence applied to adiponitrile produces the cyclic bis-phosphorane 9a.The previously unknown hydrocarbon 1,3,9,11-cyclohexadecatetraene (12) has been prepared from 8a and adipoaldehyde.

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