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114524-26-4

2H-Pyran, tetrahydro-2-methyl-3-(phenylseleno)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 114524-26-4 Structure

  • Basic information

    1. Product Name: 2H-Pyran, tetrahydro-2-methyl-3-(phenylseleno)-
    2. Synonyms:
    3. CAS NO:114524-26-4
    4. Molecular Formula: C12H16OSe
    5. Molecular Weight: 255.218
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 114524-26-4.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: 2H-Pyran, tetrahydro-2-methyl-3-(phenylseleno)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2H-Pyran, tetrahydro-2-methyl-3-(phenylseleno)-(114524-26-4)
    11. EPA Substance Registry System: 2H-Pyran, tetrahydro-2-methyl-3-(phenylseleno)-(114524-26-4)

  • 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: 114524-26-4(Hazardous Substances Data)

114524-26-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 114524-26-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,5,2 and 4 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 114524-26:
(8*1)+(7*1)+(6*4)+(5*5)+(4*2)+(3*4)+(2*2)+(1*6)=94
94 % 10 = 4
So 114524-26-4 is a valid CAS Registry Number.

114524-26-4Downstream Products

114524-26-4Relevant articles and documents

Automated Electrochemical Selenenylations

Amri, Nasser,Wirth, Thomas

, p. 1751 - 1761 (2020)

Integrated electrochemical reactors in automated flow systems were utilised for selenenylation reactions. The automation allowed multiple electrochemical reactions of a programmed sequence to be performed in a fully autonomous way. Many functionalised selenenylated products were synthesised in short reaction times in good to high yields.

An efficient route to phenylselenoethers in the presence of Ag2O

Bugarcic, Zorica M.,Divac, Vera M.,Gavrilovic, Mariana P.

, p. 985 - 988 (2008/03/17)

An efficient protocol for the preparation of phenylselenoethers from unsaturated alcohols using phenylselenenyl halides at room temperature was developed. The procedure employs phenylselenenyl chloride and bromide, some Δ 4- and Δ 5-

Studies of the reactions of some benzenalkenyl ethers with benzenselenenyl halides

Bugar?i?, Zorica,Konstantinovi?, Stanimir,Mojsilovi?, Biljana

, p. 728 - 731 (2007/10/03)

Intramolecular cyclization of some benzenalkenyl ethers with benzenselenenyl halides (PhSeX, X=Cl and Br) at different temperatures (- 78°C, 0°C and room temperature) has been investigated. It has been found that Δ4-alkenyl benzyl ethers. affor

ELECTROCHEMICAL CYCLIZATION OF UNSATURATED HYDROXY COMPOUNDS. PART I. PHENYLSELENOETHERIFICATION

Mihailovic, M. Lj.,Konstantinovic, S.,Vukicevic, R.

, p. 4343 - 4346 (2007/10/02)

One-step cyclization of alkenols has been accomplished by electrooxidative phenylselenoetherification.The reaction was performed by electrolysis of unsaturated alcohols and diphenyl diselenide in methylene chloride containing tetraethylammonium bromide.

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