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1231909-02-6

rac-FeC10H7(CH(CH3)CH2CHPiPr2)(PPh2) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1231909-02-6 Structure

  • Basic information

    1. Product Name: rac-FeC10H7(CH(CH3)CH2CHPiPr2)(PPh2)
    2. Synonyms:
    3. CAS NO:1231909-02-6
    4. Molecular Formula:
    5. Molecular Weight: 540.448
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1231909-02-6.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: rac-FeC10H7(CH(CH3)CH2CHPiPr2)(PPh2)(CAS DataBase Reference)
    10. NIST Chemistry Reference: rac-FeC10H7(CH(CH3)CH2CHPiPr2)(PPh2)(1231909-02-6)
    11. EPA Substance Registry System: rac-FeC10H7(CH(CH3)CH2CHPiPr2)(PPh2)(1231909-02-6)

  • 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: 1231909-02-6(Hazardous Substances Data)

1231909-02-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1231909-02-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,1,9,0 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1231909-02:
(9*1)+(8*2)+(7*3)+(6*1)+(5*9)+(4*0)+(3*9)+(2*0)+(1*2)=126
126 % 10 = 6
So 1231909-02-6 is a valid CAS Registry Number.

1231909-02-6Downstream Products

1231909-02-6Relevant articles and documents

Synthesis and characterization of [3]ferrocenophane-derived P, P-chelate ligand gold complexes featuring an aurophilic interaction

Luebbe, Gerrit,Nilewski, Christian,Kehr, Gerald,Froehlich, Roland,Erker, Gerhard

, p. 1413 - 1422 (2009)

The P, P-chelate ligand (rac)-4 was prepared starting from the α-dimethylamino-[3]ferroceno-phane by a series of directed ortho-lithiation, phosphination with ClPPh2 and substituent exchange using HPiPr2. Treatment with tw

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