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Phosphonic acid, methyl-, 2,2-dimethylpropyl phenyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • Phosphonic acid, methyl-, 2,2-dimethylpropyl phenyl ester

    Cas No: 88065-74-1

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  • 88065-74-1 Structure
  • Basic information

    1. Product Name: Phosphonic acid, methyl-, 2,2-dimethylpropyl phenyl ester
    2. Synonyms:
    3. CAS NO:88065-74-1
    4. Molecular Formula: C12H19O3P
    5. Molecular Weight: 242.255
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 88065-74-1.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: Phosphonic acid, methyl-, 2,2-dimethylpropyl phenyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: Phosphonic acid, methyl-, 2,2-dimethylpropyl phenyl ester(88065-74-1)
    11. EPA Substance Registry System: Phosphonic acid, methyl-, 2,2-dimethylpropyl phenyl ester(88065-74-1)
  • 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: 88065-74-1(Hazardous Substances Data)

88065-74-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88065-74-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,0,6 and 5 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 88065-74:
(7*8)+(6*8)+(5*0)+(4*6)+(3*5)+(2*7)+(1*4)=161
161 % 10 = 1
So 88065-74-1 is a valid CAS Registry Number.

88065-74-1Downstream Products

88065-74-1Relevant articles and documents

Quasiphosphonium Intermediates. Part 3. Preparation, Structure, and Reactivity of Alkoxyphosphonium Halides in the Reaction of Neopentyl Diphenylphosphinite, Dineopentyl Phenylphosphinite, and Trineopentyl Phosphite with Halogenomethanes and the Effect of Phenoxy-substituenst on the ...

Hudson, Harry R.,Kow, Aloysius,Roberts, John C.

, p. 1363 - 1368 (2007/10/02)

The reactions of neopenthyl diphenylphosphinite with chloro-, bromo-, or iodo-methane and of dineopentyl phenylphosphphonite with bromo- or iodo-methane yield crystalline alkoxyphosphonium halides.In deuteriochloroform these intermediates decompose by a first-order process which involves rate-determining collapse of the phosphonium halide ion-pair with SN2-type fission of the alkyl-oxygen bond.Rates for chloride, bromide, and iodide are similar.In a more ionising medium (deuterioacetonitrile) dissociation leads to stabilisation of the intermediates and to deviation from first-order decomposition.Previously determined X-ray diffraction data for the bromides, together with relative rates of decomposition in deuteriochloroform for intermediates in the series Phn(RO)3-nP+MeX- (n = 0,1, or 2) suggest that the stability and reactivity of alkoxyphosphonium intermediates are determined largely by inductive rather than mesomeric effects of ligands.The presence of phenoxy-substituents on phosphorus may cause a tendency towards SN1-type fission of the alkyl-oxygen bond in certain circumstances.

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