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2-(diphenylphosphinoyl)-1-iodo-3-phenylethynylnaphthalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1388770-89-5 Structure
  • Basic information

    1. Product Name: 2-(diphenylphosphinoyl)-1-iodo-3-phenylethynylnaphthalene
    2. Synonyms: 2-(diphenylphosphinoyl)-1-iodo-3-phenylethynylnaphthalene
    3. CAS NO:1388770-89-5
    4. Molecular Formula:
    5. Molecular Weight: 554.366
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1388770-89-5.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-(diphenylphosphinoyl)-1-iodo-3-phenylethynylnaphthalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(diphenylphosphinoyl)-1-iodo-3-phenylethynylnaphthalene(1388770-89-5)
    11. EPA Substance Registry System: 2-(diphenylphosphinoyl)-1-iodo-3-phenylethynylnaphthalene(1388770-89-5)
  • 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: 1388770-89-5(Hazardous Substances Data)

1388770-89-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1388770-89-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,8,7,7 and 0 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1388770-89:
(9*1)+(8*3)+(7*8)+(6*8)+(5*7)+(4*7)+(3*0)+(2*8)+(1*9)=225
225 % 10 = 5
So 1388770-89-5 is a valid CAS Registry Number.

1388770-89-5Relevant articles and documents

3,3′-Substituted BINAP derivatives containing C-bound substituents: Applications in asymmetric hydrogenation reactions

Rankic, Danica A.,Parvez, Masood,Keay, Brian A.

, p. 754 - 763 (2012)

The synthesis and resolution of the first 3,3′-disubstituted BINAP ligands containing C-bonded substituents are described. An ortho-metallation/ electrophile capture sequence was used to obtain the key trisubstituted naphthalene intermediate available and this intermediate was successfully converted into the desired ligands. Minor changes in the steric and stereoelectronic components of the 3,3′-substituents on the enantioselectivity and product enantiosense were also assessed in the context of the Rh-catalyzed asymmetric hydrogenation of enamides. A comparison of the absolute stereochemistry of the products derived from 3,3′-disubstituted BINAPs containing C-bonded substituents with their O-bound counterparts indicated that the product enantiosense could be dictated by increased steric bulk due to the 3 and 3′-substituents.

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