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(E)-4-(4-methoxyphenyl)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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  • 1182278-37-0 Structure
  • Basic information

    1. Product Name: (E)-4-(4-methoxyphenyl)but-3-ene-1,2-diyl diacetate
    2. Synonyms: (E)-4-(4-methoxyphenyl)but-3-ene-1,2-diyl diacetate
    3. CAS NO:1182278-37-0
    4. Molecular Formula:
    5. Molecular Weight: 278.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1182278-37-0.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-methoxyphenyl)but-3-ene-1,2-diyl diacetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: (E)-4-(4-methoxyphenyl)but-3-ene-1,2-diyl diacetate(1182278-37-0)
    11. EPA Substance Registry System: (E)-4-(4-methoxyphenyl)but-3-ene-1,2-diyl diacetate(1182278-37-0)
  • 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: 1182278-37-0(Hazardous Substances Data)

1182278-37-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1182278-37-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,2,2,7 and 8 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1182278-37:
(9*1)+(8*1)+(7*8)+(6*2)+(5*2)+(4*7)+(3*8)+(2*3)+(1*7)=160
160 % 10 = 0
So 1182278-37-0 is a valid CAS Registry Number.

1182278-37-0Downstream Products

1182278-37-0Relevant 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

, p. 3642 - 3645 (2009)

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.

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