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CAS

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118878-05-0

8-phenyl-2,5-octanedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 118878-05-0 Structure

  • Basic information

    1. Product Name: 8-phenyl-2,5-octanedione
    2. Synonyms: 8-phenyl-2,5-octanedione
    3. CAS NO:118878-05-0
    4. Molecular Formula:
    5. Molecular Weight: 218.296
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118878-05-0.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: 8-phenyl-2,5-octanedione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8-phenyl-2,5-octanedione(118878-05-0)
    11. EPA Substance Registry System: 8-phenyl-2,5-octanedione(118878-05-0)

  • 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: 118878-05-0(Hazardous Substances Data)

118878-05-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118878-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,8,7 and 8 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 118878-05:
(8*1)+(7*1)+(6*8)+(5*8)+(4*7)+(3*8)+(2*0)+(1*5)=160
160 % 10 = 0
So 118878-05-0 is a valid CAS Registry Number.

118878-05-0Downstream Products

118878-05-0Relevant articles and documents

Hydroacylation of Simple Alkyl Vinyl Ketones Using Organotetracarbonylferrates

Yamashita, Masakazu,Tashika, Haruyoshi,Suemitsu, Rikisaku

, p. 691 - 692 (1989)

Alkyl vinyl ketones were hydroacylated by organotetracarbonylferrates to the corresponding 1,4-diketones in good yields in dipolar aprotic solvents such as dimethylacetamide.The addition of 18-Crown-6 made an increase of the yields.

Ruthenium-catalyzed three-component coupling via hydrative conjugate addition of alkynes to alkenes: One-pot synthesis of 1,4-dicarbonyl compounds

Chen, Yiyun,Park, Sung Hwan,Lee, Chung Whan,Lee, Chulbom

supporting information; experimental part, p. 2000 - 2004 (2011/11/07)

A catalytic three-way rendezvous: Terminal alkynes undergo metal vinylidene formation, anti-Markovnikov hydration to give a metal acyl complex, and conjugate addition to produce synthetically useful 1,4-dicarbonyl compounds under ruthenium catalysis. This one-pot three-component coupling reaction is a useful platform for further exploration in alkyne functionalization.

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