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94866-47-4

1,7-Diphenyl-4-acetyl-heptadiin-(1,6) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 94866-47-4 Structure

  • Basic information

    1. Product Name: 1,7-Diphenyl-4-acetyl-heptadiin-(1,6)
    2. Synonyms: 1,7-Diphenyl-4-acetyl-heptadiin-(1,6)
    3. CAS NO:94866-47-4
    4. Molecular Formula:
    5. Molecular Weight: 286.373
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 94866-47-4.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: 1,7-Diphenyl-4-acetyl-heptadiin-(1,6)(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,7-Diphenyl-4-acetyl-heptadiin-(1,6)(94866-47-4)
    11. EPA Substance Registry System: 1,7-Diphenyl-4-acetyl-heptadiin-(1,6)(94866-47-4)

  • 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: 94866-47-4(Hazardous Substances Data)

94866-47-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 94866-47-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,4,8,6 and 6 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 94866-47:
(7*9)+(6*4)+(5*8)+(4*6)+(3*6)+(2*4)+(1*7)=184
184 % 10 = 4
So 94866-47-4 is a valid CAS Registry Number.

94866-47-4Downstream Products

94866-47-4Relevant articles and documents

Ruthenium-catalyzed hydrocarbamoylative cyclization of 1,6-diynes with formamides

Mori, Shota,Shibuya, Masatoshi,Yamamoto, Yoshihiko

, p. 207 - 210 (2017)

The ruthenium-catalyzed hydrocarbamoylative cyclization of 1,6-diynes with formamides afforded exocyclic-diene-type α,β,γ,δ-unsaturated amides with 100% stereoselectivity. A plausible mechanism involving ruthenium hydride species is proposed to explain the experimental results. Some control experiments, performed using DMF-d7 and/or D2O, corroborate the proposed mechanism.

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