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1-tert-butyldimethylsilyloxy-2-ethyl-1-cyclohexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1389334-08-0 Structure
  • Basic information

    1. Product Name: 1-tert-butyldimethylsilyloxy-2-ethyl-1-cyclohexene
    2. Synonyms:
    3. CAS NO:1389334-08-0
    4. Molecular Formula:
    5. Molecular Weight: 240.461
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1389334-08-0.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: 1-tert-butyldimethylsilyloxy-2-ethyl-1-cyclohexene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-tert-butyldimethylsilyloxy-2-ethyl-1-cyclohexene(1389334-08-0)
    11. EPA Substance Registry System: 1-tert-butyldimethylsilyloxy-2-ethyl-1-cyclohexene(1389334-08-0)
  • 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: 1389334-08-0(Hazardous Substances Data)

1389334-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1389334-08-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,9,3,3 and 4 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1389334-08:
(9*1)+(8*3)+(7*8)+(6*9)+(5*3)+(4*3)+(3*4)+(2*0)+(1*8)=190
190 % 10 = 0
So 1389334-08-0 is a valid CAS Registry Number.

1389334-08-0Downstream Products

1389334-08-0Relevant articles and documents

Facile isomerization of silyl enol ethers catalyzed by triflic imide and its application to one-pot isomerization-(2 + 2) cycloaddition

Inanaga, Kazato,Ogawa, Yu,Nagamoto, Yuuki,Daigaku, Akihiro,Tokuyama, Hidetoshi,Takemoto, Yoshiji,Takasu, Kiyosei

, p. 658 - 661 (2012)

A triflic imide (Tf2NH) catalyzed isomerization of kinetically favourable silyl enol ethers into thermodynamically stable ones was developed. We also demonstrated a one-pot catalytic reaction consisting of (2 + 2) cycloaddition and isomerization. In the reaction sequence, Tf2NH catalyzes both of the reactions.

Copper-Catalyzed Formal Dehydrogenative Coupling of Carbonyls with Polyfluoroarenes Leading to β-C-H Arylation

Xie, Weilong,Kim, Dongwook,Chang, Sukbok

supporting information, p. 20588 - 20593 (2020/12/23)

We herein communicate a formal dehydrogenative coupling of carbonyls with polyfluoroarenes enabled by Cu catalysis. Silyl enol ethers initially prepared from carbonyls are postulated to undergo the copper-mediated oxidative dehydrogenative coupling with polyfluoroarenes via a radical pathway. Including cyclic and linear ketones, aldehydes, and esters, a broad range of β-aryl carbonyl products were efficiently obtained in high regio- and stereoselectivity with excellent functional group tolerance.

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