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(2-Pyridylthio)phenyl selenide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124201-01-0 Structure
  • Basic information

    1. Product Name: (2-Pyridylthio)phenyl selenide
    2. Synonyms: (2-Pyridylthio)phenyl selenide
    3. CAS NO:124201-01-0
    4. Molecular Formula:
    5. Molecular Weight: 266.225
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124201-01-0.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: (2-Pyridylthio)phenyl selenide(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-Pyridylthio)phenyl selenide(124201-01-0)
    11. EPA Substance Registry System: (2-Pyridylthio)phenyl selenide(124201-01-0)
  • 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: 124201-01-0(Hazardous Substances Data)

124201-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124201-01-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,2,0 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124201-01:
(8*1)+(7*2)+(6*4)+(5*2)+(4*0)+(3*1)+(2*0)+(1*1)=60
60 % 10 = 0
So 124201-01-0 is a valid CAS Registry Number.

124201-01-0Downstream Products

124201-01-0Relevant articles and documents

Chemistry of Amidyl Radicals Produced from N-Hydroxypyridine-2-thione Imidate Esters

Esker, John L.,Newcomb, Martin

, p. 4933 - 4940 (1993)

The title radicals precursors were prepared from secondary amides by reaction of the amide with phosgene to give an imidoyl chloride followed by reaction with the sodium salt of N-hydroxypyridine-2-thione.Visible light initiated reactions of these precursors gave amidyl radicals 2 which could react with their precursors to give N-(2-pyridylthio) amides or with t-BuSH to give the parent amide.Radicals 2 containing δ,ε-unsaturation on the acyl or alkyl chain cyclized in a 5-exo fashion to give ultimately γ-lactams and N-acylpyrrolidines, respectively.Tandem 5-exo cyclizations of the N-allyl-4-pentenamidyl radical gave pyrrolizidinone products, and a tandem 5-exo/6-endo reaction sequence of the N-(4-pentenyl)benzamidyl radical gave, ultimately, 3,4-benzoindolizidinone.Several relative rate constants for cyclization and trapping of the amidyl radicals and for intramolecular reactions and trapping of the carbon-centered radicals formed by amidyl radical cyclizations were determined, and these values can be employed in synthetic planning.

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