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CAS

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97826-86-3

(E)-1-(2-butoxyethenyl)-4-nitrobenzene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 97826-86-3 Structure

  • Basic information

    1. Product Name: (E)-1-(2-butoxyethenyl)-4-nitrobenzene
    2. Synonyms: (E)-1-(2-butoxyethenyl)-4-nitrobenzene
    3. CAS NO:97826-86-3
    4. Molecular Formula:
    5. Molecular Weight: 221.256
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 97826-86-3.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: (E)-1-(2-butoxyethenyl)-4-nitrobenzene(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-1-(2-butoxyethenyl)-4-nitrobenzene(97826-86-3)
    11. EPA Substance Registry System: (E)-1-(2-butoxyethenyl)-4-nitrobenzene(97826-86-3)

  • 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: 97826-86-3(Hazardous Substances Data)

97826-86-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97826-86-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,8,2 and 6 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97826-86:
(7*9)+(6*7)+(5*8)+(4*2)+(3*6)+(2*8)+(1*6)=193
193 % 10 = 3
So 97826-86-3 is a valid CAS Registry Number.

97826-86-3Downstream Products

97826-86-3Relevant articles and documents

α-Regioselectivity in Palladium-Catalyzed Arylation of Acyclic Enol Ethers

Cabri, Walter,Candiani, Ilaria,Bedeschi, Angelo,Penco, Sergio,Santi, Roberto

, p. 1481 - 1486 (2007/10/02)

Regioselective α-arylation of acyclic enol ethers by aryl trifluoromethanesulfonates, aryl bromide, aryl iodides, and aroyl chlorides is described.The outcome of the reaction proved to be dependent from the relationship between ligand and counterion in the oxidative complex.

Synthesis of β-Arylvinyl Ethers by the Palladium-Catalyzed Reaction of Aroyl Chlorides with Vinyl Ethers

Andersson, Carl-Magnus,Hallberg, Anders

, p. 235 - 239 (2007/10/02)

Reaction of aroyl chlorides with butyl vinyl ether in the presence of a palladium catalyst and an amine base affords β-arylvinyl ethers in 40-60percent yield.Both with regard to regioselectivity and reaction rate, aroyl chlorides were superior to aryl bro

Regiochemistry of Palladium-Catalyzed Arylation Reactions of Enol Ethers. Electronic Control of Selection for α- or β-Arylation

Andersson, Carl-Magnus,Hallberg, Anders,Daves, G. Doyle

, p. 3529 - 3536 (2007/10/02)

The regiochemistry of palladium-mediated arylation Heck arylation) of enol ethers is sensitive to (a) the structure of the enol ether, (b) the arylating agent used, and (c) the reaction medium-catalyst system.By control of these parameters a 50-fold varia

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