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87274-28-0

methyl 4-oxo-7,7-diphenylhept-6-enoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 87274-28-0 Structure

  • Basic information

    1. Product Name: methyl 4-oxo-7,7-diphenylhept-6-enoate
    2. Synonyms: methyl 4-oxo-7,7-diphenylhept-6-enoate
    3. CAS NO:87274-28-0
    4. Molecular Formula:
    5. Molecular Weight: 308.377
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87274-28-0.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: methyl 4-oxo-7,7-diphenylhept-6-enoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 4-oxo-7,7-diphenylhept-6-enoate(87274-28-0)
    11. EPA Substance Registry System: methyl 4-oxo-7,7-diphenylhept-6-enoate(87274-28-0)

  • 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: 87274-28-0(Hazardous Substances Data)

87274-28-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87274-28-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,7 and 4 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87274-28:
(7*8)+(6*7)+(5*2)+(4*7)+(3*4)+(2*2)+(1*8)=160
160 % 10 = 0
So 87274-28-0 is a valid CAS Registry Number.

87274-28-0Downstream Products

87274-28-0Relevant articles and documents

Photoinduced α-Alkenylation of Katritzky Salts: Synthesis of β,?-Unsaturated Esters

Zhang, Chao-Shen,Bao, Lei,Chen, Kun-Quan,Wang, Zhi-Xiang,Chen, Xiang-Yu

, p. 1577 - 1581 (2021)

?,?-Unsaturated esters are building blocks in biologically important compounds, pharmaceuticals, and natural products. Because the current synthetic methods often require transition-metal catalysts or lack general variants, we herein describe a simple NaI-involved photoinduced deaminative alkenylation for their synthesis in the absence of photocatalysts and additives. The density functional theory study unveils that the electrostatic interaction of NaI with Katritzky salts is the key to forming the photoactive electron donor-acceptor complex, thus leading to the alkyl radicals for the alkenylation.

PHOTOLYSIS OF 2,3-EPOXY-7,7-DIPHENYLBICYCLOHEPTAN-6-ONES AND 2-exo, 3-exo-DIHYDROXY-7,7-DIPHENYLBICYCLOHEPTAN-6-ONE

Davies, H. Geoff,Rahman, Shahzad S.,Roberts, Stanley M.,Wakefield, Basil J.,Winders, John A.

, p. 85 - 90 (2007/10/02)

Photolysis of 2,3-endo-epoxy-7,7-diphenylbicycloheptan-6-one ( 2 ) in methanol gave products ( 4 ), ( 8 ) derived from an oxacarbene intermediate and the products ( 5 ) - ( 7 ), ( 9 ) derived from an initially formed alkenylketene.Photolysis of the

PHOTOCHEMISTRY OF α,α-DISUBSTITUTED BICYCLIC CYCLOBUTANONES - A POTENTIAL THERMAL-PHOTOCHEMICAL METATHESIS REACTION

Lee-Ruff, Edward,Hopkinson, Alan C.,Kazarians-Moghaddam, Hira

, p. 2067 - 2070 (2007/10/02)

Under certain conditions the photolysis of α,α-disubstituted cyclobutanones give terminal olefinic esters.A two-stage thermal photochemical metathesis is described.

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