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bis(m-bromophenyl)phosphinous acid is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 108142-54-7 Structure
  • Basic information

    1. Product Name: bis(m-bromophenyl)phosphinous acid
    2. Synonyms:
    3. CAS NO:108142-54-7
    4. Molecular Formula:
    5. Molecular Weight: 359.985
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 108142-54-7.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: bis(m-bromophenyl)phosphinous acid(CAS DataBase Reference)
    10. NIST Chemistry Reference: bis(m-bromophenyl)phosphinous acid(108142-54-7)
    11. EPA Substance Registry System: bis(m-bromophenyl)phosphinous acid(108142-54-7)
  • 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: 108142-54-7(Hazardous Substances Data)

108142-54-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 108142-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,8,1,4 and 2 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 108142-54:
(8*1)+(7*0)+(6*8)+(5*1)+(4*4)+(3*2)+(2*5)+(1*4)=97
97 % 10 = 7
So 108142-54-7 is a valid CAS Registry Number.

108142-54-7Relevant articles and documents

Rhodium(III)-Catalyzed Enantiotopic C?H Activation Enables Access to P-Chiral Cyclic Phosphinamides

Sun, Yang,Cramer, Nicolai

, p. 364 - 367 (2017)

Compounds with stereogenic phosphorus atoms are frequently used as ligands for transition-metal as well as organocatalysts. A direct catalytic enantioselective method for the synthesis of P-chiral compounds from easily accessible diaryl phosphinamides is presented. The use of rhodium(III) complexes equipped with a suitable atropochiral cyclopentadienyl ligand is shown to enable an enantiodetermining C?H activation step. Upon trapping with alkynes, a broad variety of cyclic phosphinamides with a stereogenic phosphorus(V) atom are formed in high yields and enantioselectivities. Moreover, these can be reduced enantiospecifically to P-chiral phosphorus(III) compounds.

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