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53909-72-1

2-bromo-1,1-dibenzylethyl hydroperoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 53909-72-1 Structure

  • Basic information

    1. Product Name: 2-bromo-1,1-dibenzylethyl hydroperoxide
    2. Synonyms: 2-bromo-1,1-dibenzylethyl hydroperoxide
    3. CAS NO:53909-72-1
    4. Molecular Formula:
    5. Molecular Weight: 321.214
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 53909-72-1.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: 2-bromo-1,1-dibenzylethyl hydroperoxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-bromo-1,1-dibenzylethyl hydroperoxide(53909-72-1)
    11. EPA Substance Registry System: 2-bromo-1,1-dibenzylethyl hydroperoxide(53909-72-1)

  • 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: 53909-72-1(Hazardous Substances Data)

53909-72-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53909-72-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,9,0 and 9 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 53909-72:
(7*5)+(6*3)+(5*9)+(4*0)+(3*9)+(2*7)+(1*2)=141
141 % 10 = 1
So 53909-72-1 is a valid CAS Registry Number.

53909-72-1Relevant articles and documents

Novel Transformations of 1,2-Dioxetanes: β-Hydroxy Ethers by Addition of Alkyllithium Reagents

Adam, Waldemar,Heil, Markus

, p. 235 - 241 (2007/10/02)

The reaction of 1,2-dioxetanes with alkyllithium reagents was investigated.The 3,3-disubstituted dioxetanes 2a,d and their halogen-substituted analogues 2b,c, which were used as probes to differentiate between the mechanistic alternatives (SN2 reactivity vs. single-electron transfer), reacted with n-BuLi to afford the β-hydroxy ethers 3a-d.Additionally, the epoxide 4 was obtained from dioxetanes 2b,c.The epoxide 5 and a small amount of acetophenone were found in the reaction of dioxetane 2c with triphenylmethyllithium, but only the minor part of the dioxetane-derived products could be identified.The observation of the epoxides 4 and 5 led to the mechanistic conclusion that nucleophilic attack (SN2 reactivity) is the most prominent process in this reaction.Key Words: Dioxetanes / Single electron transfer vs. nucleophilic attack / Ethers, β-hydroxy / Alkyllithium reagents

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