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908127-23-1

tris-(4-oct-7-enyloxy-phenyl)-phosphane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 908127-23-1 Structure

  • Basic information

    1. Product Name: tris-(4-oct-7-enyloxy-phenyl)-phosphane
    2. Synonyms: tris-(4-oct-7-enyloxy-phenyl)-phosphane
    3. CAS NO:908127-23-1
    4. Molecular Formula:
    5. Molecular Weight: 640.887
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 908127-23-1.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: tris-(4-oct-7-enyloxy-phenyl)-phosphane(CAS DataBase Reference)
    10. NIST Chemistry Reference: tris-(4-oct-7-enyloxy-phenyl)-phosphane(908127-23-1)
    11. EPA Substance Registry System: tris-(4-oct-7-enyloxy-phenyl)-phosphane(908127-23-1)

  • 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: 908127-23-1(Hazardous Substances Data)

908127-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 908127-23-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,1,2 and 7 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 908127-23:
(8*9)+(7*0)+(6*8)+(5*1)+(4*2)+(3*7)+(2*2)+(1*3)=161
161 % 10 = 1
So 908127-23-1 is a valid CAS Registry Number.

908127-23-1Relevant articles and documents

"Giant" gyroscope-like molecules consisting of dipolar Cl-Rh-CO rotators encased in three-spoke stators that define 25-27-membered macrocycles

Wang, Leyong,Hampel, Frank,Gladysz, John A.

, p. 4372 - 4375 (2007/10/03)

(Chemical Equation Presented) Yet another feat for the Crubbs catalyst: Reactions with 1a,b followed by hydrogenations give 2a,b. The sizeable cavities of 2, which were characterized crystallographically, allow for rapid Cl-Rh-CO rotation in solution. Reactions with ArC≡CLi give ArC≡C-Rh-CO species; when the aryl group is sufficiently large, it is confined between two macrocycles, blocking rotation.

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