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CAS

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80765-36-2

2-oxo-2-(p-nitrophenoxy)-1,3-dioxa-2-phospha-6-methyl-6-azacyclooctane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 80765-36-2 Structure

  • Basic information

    1. Product Name: 2-oxo-2-(p-nitrophenoxy)-1,3-dioxa-2-phospha-6-methyl-6-azacyclooctane
    2. Synonyms: 2-oxo-2-(p-nitrophenoxy)-1,3-dioxa-2-phospha-6-methyl-6-azacyclooctane
    3. CAS NO:80765-36-2
    4. Molecular Formula:
    5. Molecular Weight: 302.224
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 80765-36-2.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-oxo-2-(p-nitrophenoxy)-1,3-dioxa-2-phospha-6-methyl-6-azacyclooctane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-oxo-2-(p-nitrophenoxy)-1,3-dioxa-2-phospha-6-methyl-6-azacyclooctane(80765-36-2)
    11. EPA Substance Registry System: 2-oxo-2-(p-nitrophenoxy)-1,3-dioxa-2-phospha-6-methyl-6-azacyclooctane(80765-36-2)

  • 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: 80765-36-2(Hazardous Substances Data)

80765-36-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80765-36-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,7,6 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 80765-36:
(7*8)+(6*0)+(5*7)+(4*6)+(3*5)+(2*3)+(1*6)=142
142 % 10 = 2
So 80765-36-2 is a valid CAS Registry Number.

80765-36-2Downstream Products

80765-36-2Relevant articles and documents

Hydrolysis of Medium-Ring Phosphates. Mechanism of Rate Acceleration by an Amino Group

Sharma, Ravinder K.,Vaidyanathaswamy, Ramamoorthy

, p. 1741 - 1745 (1982)

A series of 2-oxo-2-(p-nitrophenoxy)-1,3-dioxa-2-phosphacyclooctane derivatives (1-5) having either a nitrogen or a sulfur atom placed transannularly in the ring were synthesized, and their rates of hydrolysis were examined.The pH-rate profile shows that while 1 undergoes hydrolysis over a wide pH range, others are hydrolyzed at a significant rate only in basic medium, thus implicating the amino function for rate enhancement.By comparison with rates obtained with 2 and 3 and the quarternary derivative 4, a mechanism involving rate-determining proton transfer from nitrogen to phosphoryl oxygen has been proposed for the hydrolysis of 1 at an acidic pH.The enhancement in the rate of spontaneous hydrolysis of the same compound, however, is explained by a combination of intramolecular general-base and nucleophilic catalysis.

Synthesis and kinetics of hydrolysis of cyclic phosphates

Sikder,Sikder

, p. 1697 - 1706 (2007/10/03)

A series of new cyclic phosphates were prepared and characterized by spectral data and elemental analyses. Hydrolysis of these compounds was carried out in both acid and basic media, and the rates were compared with the cyclic phosphates without an alpha

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