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4-phenylbut-3-yn-1-yl acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 85655-96-5 Structure
  • Basic information

    1. Product Name: 4-phenylbut-3-yn-1-yl acetate
    2. Synonyms: 4-phenylbut-3-yn-1-yl acetate
    3. CAS NO:85655-96-5
    4. Molecular Formula:
    5. Molecular Weight: 188.226
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 85655-96-5.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: 4-phenylbut-3-yn-1-yl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-phenylbut-3-yn-1-yl acetate(85655-96-5)
    11. EPA Substance Registry System: 4-phenylbut-3-yn-1-yl acetate(85655-96-5)
  • 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: 85655-96-5(Hazardous Substances Data)

85655-96-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85655-96-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,6,5 and 5 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 85655-96:
(7*8)+(6*5)+(5*6)+(4*5)+(3*5)+(2*9)+(1*6)=175
175 % 10 = 5
So 85655-96-5 is a valid CAS Registry Number.

85655-96-5Relevant articles and documents

Direct Conversion of Internal Alkynes into α-Iodoenones: One-Step Collaborative Iodination and Oxidation

Wang, Youliang,Genoux, Alexandre,Ghorai, Subir,Chen, Hongyi,Todd, Robert,Zhang, Liming

supporting information, p. 1417 - 1420 (2016/05/19)

The reaction of an internal alkyne with 2,6-dichloropyridine N-oxide, a nucleophilic oxidant, and electrophilic N-iodosuccinimide (NIS) simultaneously enables the direct access to versatile α-iodoenones. Electronically biased internal alkynes undergo the one-step transformation with excellent regioselectivities and with practical Z/E ratios. In comparison to the related oxidative gold catalysis using pyridine N-oxides, this reaction employs NIS as the stoichiometric ynophile instead of the soft acidic noble metal catalyst and affords products featuring an additional versatile C-I bond. Similar strategies for replacing ynophilic cationic gold(I) complexes in oxidative gold catalysis with likewise ynophilic stoichiometric electrophiles would enable the development of new synthetic methods.

HOMOGENEOUS METATHESIS OF FUNCTIONALISED ACETYLENES

Villemin, Didier,Cadiot, Paul

, p. 5139 - 5140 (2007/10/02)

The first examples of functionalised acetylenes metathesis are described: (1) using molybdenum carbonyl-phenol complexes gave the expected tolane (2) and disubstituted acetylene (3).

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