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99485-24-2

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

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  • 99485-24-2 Structure

  • Basic information

    1. Product Name: 2-phenylseleno-2-butenal
    2. Synonyms: 2-phenylseleno-2-butenal
    3. CAS NO:99485-24-2
    4. Molecular Formula:
    5. Molecular Weight: 225.149
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 99485-24-2.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-phenylseleno-2-butenal(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-phenylseleno-2-butenal(99485-24-2)
    11. EPA Substance Registry System: 2-phenylseleno-2-butenal(99485-24-2)

  • 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: 99485-24-2(Hazardous Substances Data)

99485-24-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 99485-24-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,4,8 and 5 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 99485-24:
(7*9)+(6*9)+(5*4)+(4*8)+(3*5)+(2*2)+(1*4)=192
192 % 10 = 2
So 99485-24-2 is a valid CAS Registry Number.

99485-24-2Upstream product

99485-24-2Downstream Products

99485-24-2Relevant articles and documents

A Versatile and Highly Selective Hypervalent Iodine (III)/ 2,2,6,6-Tetraniethyl-1-piperidinyloxyl-Mediated Oxidation of Alcohols to Carbonyl Compounds

De Mico, Antonella,Margarita, Roberto,Parlanti, Luca,Vescovi, Andrea,Piancatelli, Giovanni

, p. 6974 - 6977 (1997)

Catalytic amounts of 2,2,6,6-tetramethyl-1-piperidinyloxyl (TEMPO) are used in combination with [bis(acetoxy)iodo]benzene (BAIB) as a stoichiometric oxidant in the conversion of primary and secondary alcohols to carbonyl compounds. This procedure works efficiently at room temperature in almost all common solvents and neat in some cases. This process exhibits a very high degree of selectivity for the oxidation of primary alcohols to aldehydes, without any noticeable overoxidation to carboxyl compounds, and a high chemoselectivity in the presence of either secondary alcohols or of other oxidizable moieties. This procedure allows an easy, convenient, high-yielding method for the oxidation of alcohols starting from commercially available compounds.

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