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82912-01-4

2-Nitro-2-phenylselenononanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 82912-01-4 Structure

  • Basic information

    1. Product Name: 2-Nitro-2-phenylselenononanol
    2. Synonyms: 2-Nitro-2-phenylselenononanol
    3. CAS NO:82912-01-4
    4. Molecular Formula:
    5. Molecular Weight: 344.313
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 82912-01-4.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-Nitro-2-phenylselenononanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-Nitro-2-phenylselenononanol(82912-01-4)
    11. EPA Substance Registry System: 2-Nitro-2-phenylselenononanol(82912-01-4)

  • 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: 82912-01-4(Hazardous Substances Data)

82912-01-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82912-01-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,9,1 and 2 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 82912-01:
(7*8)+(6*2)+(5*9)+(4*1)+(3*2)+(2*0)+(1*1)=124
124 % 10 = 4
So 82912-01-4 is a valid CAS Registry Number.

82912-01-4Downstream Products

82912-01-4Relevant articles and documents

Intramolecular conjugate displacement: A general route to hexahydroquinolizines, hexahydroindolizines, and related [m,n,0]-bicyclic structures with nitrogen at a bridgehead

Clive, Derrick L. J.,Li, Zhiyong,Yu, Maolin

, p. 5608 - 5617 (2008/02/09)

(Chemical Equation Presented) N-Protected amino aldehydes can be converted into allylic alcohols by the classical Morita-Baylis-Hillman reaction (cf. 2 → 3) or by condensation with selenium-stabilized carbanions, followed by oxidation (cf. 2 → 8 → 3). The

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