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332041-60-8

Cyclohexanone trimethoxysilyl enol ether is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 332041-60-8 Structure

  • Basic information

    1. Product Name: Cyclohexanone trimethoxysilyl enol ether
    2. Synonyms: Cyclohexanone trimethoxysilyl enol ether
    3. CAS NO:332041-60-8
    4. Molecular Formula:
    5. Molecular Weight: 218.325
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 332041-60-8.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: Cyclohexanone trimethoxysilyl enol ether(CAS DataBase Reference)
    10. NIST Chemistry Reference: Cyclohexanone trimethoxysilyl enol ether(332041-60-8)
    11. EPA Substance Registry System: Cyclohexanone trimethoxysilyl enol ether(332041-60-8)

  • 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: 332041-60-8(Hazardous Substances Data)

332041-60-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 332041-60-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,0,4 and 1 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 332041-60:
(8*3)+(7*3)+(6*2)+(5*0)+(4*4)+(3*1)+(2*6)+(1*0)=88
88 % 10 = 8
So 332041-60-8 is a valid CAS Registry Number.

332041-60-8Relevant articles and documents

BINAP/AgOTf/KF/18-crown-6 as new bifunctional catalysts for asymmetric Sakurai-Hosomi allylation and Mukaiyama aldol reaction

Wadamoto, Manabu,Ozasa, Nobuko,Yanagisawa, Akira,Yamamoto, Hisashi

, p. 5593 - 5601 (2003)

A catalytic amount of KF·18-crown-6 complex is effective as a soluble fluoride source to activate an asymmetric Sakurai-Hosomi allylation with BINAP and silver(I) triflate catalyst. The allylation of a variety of aromatic, α,β-unsaturated and aliphatic al

Chiral base-catalyzed aldol reaction of trimethoxysilyl enol ethers: Effect of water as an additive on stereoselectivities

Orito, Yuya,Hashimoto, Shunichi,Ishizuka, Tadao,Nakajima, Makoto

, p. 390 - 400 (2007/10/03)

An aldol reaction of trimethoxysilyl enol ether catalyzed by lithium binaphtholate is described. The aldol reaction of trimethoxysilyl enol ether derived from cyclohexanone under anhydrous conditions predominantly afforded the anti-aldol adduct with moder

Enantioselective aldol reaction of trimethoxysilyl enol ethers with aldehydes catalyzed by p-Tol-BINAP·AgF complex

Yanagisawa,Nakatsuka,Asakawa,Kageyama,Yamamoto

, p. 69 - 72 (2007/10/03)

New catalytic asymmetric Mukaiyama-type aldol reaction using trimethoxysilyl enol ethers was achieved using p-Tol-BINAP·AgF complex as a catalyst. High syn- and enantioselectivities were obtained both from the E- and Z-silyl enol ethers.

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