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3,3,4,4,5,5,5-heptafluoro-1-phenyl-1-pentyne is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81674-08-0 Structure
  • Basic information

    1. Product Name: 3,3,4,4,5,5,5-heptafluoro-1-phenyl-1-pentyne
    2. Synonyms: 3,3,4,4,5,5,5-heptafluoro-1-phenyl-1-pentyne
    3. CAS NO:81674-08-0
    4. Molecular Formula:
    5. Molecular Weight: 270.15
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81674-08-0.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: 3,3,4,4,5,5,5-heptafluoro-1-phenyl-1-pentyne(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3,3,4,4,5,5,5-heptafluoro-1-phenyl-1-pentyne(81674-08-0)
    11. EPA Substance Registry System: 3,3,4,4,5,5,5-heptafluoro-1-phenyl-1-pentyne(81674-08-0)
  • 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: 81674-08-0(Hazardous Substances Data)

81674-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81674-08-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,6,7 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81674-08:
(7*8)+(6*1)+(5*6)+(4*7)+(3*4)+(2*0)+(1*8)=140
140 % 10 = 0
So 81674-08-0 is a valid CAS Registry Number.

81674-08-0Downstream Products

81674-08-0Relevant articles and documents

Synthesis of fluoroalkylated alkynes: Via visible-light photocatalysis

Iqbal, Naila,Iqbal, Naeem,Han, Sung Su,Cho, Eun Jin

, p. 1758 - 1762 (2019/02/20)

Fluoroalkylated alkynes, which are versatile building blocks for the synthesis of various biologically active organofluorine compounds, were synthesized from easily available alkynyl halides and fluoroalkyl halides by visible-light photocatalysis. Addition of fluoroalkyl radicals to alkynes and subsequent dehalogenation selectively yielded fluoroalkylated alkynes.

Oxidative coupling of radicals in reactions of compounds of tervalent iodine with trimethylsilyl(phenyl)acetylene

Lermontov,Velikohat'ko,Zefirov

, p. 977 - 978 (2007/10/03)

Reactions of trimethylsilyl(phenyl)acetylene with aryl and alkyl difluoroiodides give coupling products of substituents in high yields.

Perfluoroalkylations of Carbanions with (Perfluoroalkyl)-phenyliodonium Triflates (FITS Reagents)

Umemoto, Teruo,Gotoh, Yoshihiko

, p. 439 - 446 (2007/10/02)

FITS reagents reacted with primary alkylmagnesium halides in THF at -78 deg C to give the corresponding perfluoroalkyl(Rf)-alkanes in moderate to good yields.But an alkyl-lithium or -copper gave a poor yield of the Rf-product.The rea

PERFLUOROALKYLATION OF CARBANIONS

Umemoto, Teruo,Kuriu, Yuriko

, p. 5197 - 5200 (2007/10/02)

A successful perfluoroalkylation of various carbanions by the use of perfluoroalkylphenyliodonium trifluoromethanesulfonate (FITS) was described.The reactivity of other perfluoroalkyliodonium salt was also examined.

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