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1-phenyl-2,3-dimethylphosphirene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 910610-00-3 Structure
  • Basic information

    1. Product Name: 1-phenyl-2,3-dimethylphosphirene
    2. Synonyms: 1-phenyl-2,3-dimethylphosphirene
    3. CAS NO:910610-00-3
    4. Molecular Formula:
    5. Molecular Weight: 162.171
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 910610-00-3.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: 1-phenyl-2,3-dimethylphosphirene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenyl-2,3-dimethylphosphirene(910610-00-3)
    11. EPA Substance Registry System: 1-phenyl-2,3-dimethylphosphirene(910610-00-3)
  • 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: 910610-00-3(Hazardous Substances Data)

910610-00-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 910610-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,6,1 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 910610-00:
(8*9)+(7*1)+(6*0)+(5*6)+(4*1)+(3*0)+(2*0)+(1*0)=113
113 % 10 = 3
So 910610-00-3 is a valid CAS Registry Number.

910610-00-3Downstream Products

910610-00-3Relevant articles and documents

Anionic ring-opening polymerization of a strained phosphirene: A route to polyvinylenephosphines

Vanderark, Lawrence A.,Clark, Timothy J.,Rivard, Eric,Manners, Ian,Slootweg, J. Chris,Lammertsma, Koop

, p. 3332 - 3333 (2006)

A strained 1-phenyl-2,3-dimethylphosphirene undergoes anionic ring-opening polymerization upon initiation with n-butyl lithium at ambient temperature to yield polyvinylenephosphine, an unsaturated organophosphorus polymer. The Royal Society of Chemistry 2

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