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C16H14(2)HO9PS2(2-)*2Na(1+) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 122865-99-0 Structure
  • Basic information

    1. Product Name: C16H14(2)HO9PS2(2-)*2Na(1+)
    2. Synonyms:
    3. CAS NO:122865-99-0
    4. Molecular Formula:
    5. Molecular Weight: 493.367
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 122865-99-0.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: C16H14(2)HO9PS2(2-)*2Na(1+)(CAS DataBase Reference)
    10. NIST Chemistry Reference: C16H14(2)HO9PS2(2-)*2Na(1+)(122865-99-0)
    11. EPA Substance Registry System: C16H14(2)HO9PS2(2-)*2Na(1+)(122865-99-0)
  • 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: 122865-99-0(Hazardous Substances Data)

122865-99-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 122865-99-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,2,8,6 and 5 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 122865-99:
(8*1)+(7*2)+(6*2)+(5*8)+(4*6)+(3*5)+(2*9)+(1*9)=140
140 % 10 = 0
So 122865-99-0 is a valid CAS Registry Number.

122865-99-0Downstream Products

122865-99-0Relevant articles and documents

Organic Chemistry in water (part II). NUCLEOPHILIC ADDITION OF WATER-SOLUBLE PHOSPHINES ON ACTIVATED OLEFINS

Larpent, Chantal,Patin, Henri

, p. 6107 - 6118 (2007/10/02)

Triphenylphosphine m-trisulfonate P(PhSO3Na)3 = TPPTS and triphenylphosphine m-monosulfonate Ph2PPhSO3Na = TPPMS react in water with α,β unsaturated acids affording hydrosoluble phosphonium salts.The conversion is quantitative because water readily protonates the carbanionic intermediate thus displacing the equilibrum towards the right.This nucleophilic addition of hydrosoluble phosphines has been extended to non water miscible activated olefins in biphasic media; depending on the pH, phosphine oxides or phosphonium salts are obtained.When the reactions are carried out in D2O, the addition products are specifically deuterated.

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