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1151782-09-0

(E)-4-(4-fluorophenyl)but-3-ene-1,2-diyl diacetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1151782-09-0 Structure

  • Basic information

    1. Product Name: (E)-4-(4-fluorophenyl)but-3-ene-1,2-diyl diacetate
    2. Synonyms: (E)-4-(4-fluorophenyl)but-3-ene-1,2-diyl diacetate
    3. CAS NO:1151782-09-0
    4. Molecular Formula:
    5. Molecular Weight: 266.269
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1151782-09-0.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: (E)-4-(4-fluorophenyl)but-3-ene-1,2-diyl diacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-4-(4-fluorophenyl)but-3-ene-1,2-diyl diacetate(1151782-09-0)
    11. EPA Substance Registry System: (E)-4-(4-fluorophenyl)but-3-ene-1,2-diyl diacetate(1151782-09-0)

  • 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: 1151782-09-0(Hazardous Substances Data)

1151782-09-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1151782-09-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,5,1,7,8 and 2 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1151782-09:
(9*1)+(8*1)+(7*5)+(6*1)+(5*7)+(4*8)+(3*2)+(2*0)+(1*9)=140
140 % 10 = 0
So 1151782-09-0 is a valid CAS Registry Number.

1151782-09-0Downstream Products

1151782-09-0Relevant articles and documents

Highly regio- and stereoselective Heck reaction of allylic esters with arenediazonium salts: Application to the synthesis of kavalactones

Moro, Angelica Venturini,Cardoso, Flavio Sega Pereira,Correia, Carlos Roque Duarte

supporting information; experimental part, p. 3642 - 3645 (2011/02/25)

Image Presented A highly efficient palladium-catalyzed Heck reaction of allylic esters with arenediazonium salts is described. The reaction proceeds under mild conditions, with excellent to total regio- and stereochemical control and with retention of the traditional leaving group. Furthermore, the generality of the present methodology is illustrated by the short total synthesis of the natural kavalactones, yangonine, (±)-methysticin, and (±)-dihydromethysticin.

Pincer complex-catalyzed redox coupling of alkenes with lodonium salts via presumed palladium(IV) itermediates

Aydin, Juhanes,Larsson, Johanna M.,Selander, Nicklas,Szabo, Kalman J.

supporting information; experimental part, p. 2852 - 2854 (2009/12/05)

Palladium pincer complexes directly catalyze the redox coupling reactions of functionalized alkenes and iodonium salts. The catalytic process, which Is suitable for mild catalytic functionalization of allylic acetates and electron-rich alkenes, probably o

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