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124414-01-3

tert-butyl[(4,4-dimethoxycyclohexyl)oxy]dimethylsilane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 124414-01-3 Structure

  • Basic information

    1. Product Name: tert-butyl[(4,4-dimethoxycyclohexyl)oxy]dimethylsilane
    2. Synonyms: tert-butyl[(4,4-dimethoxycyclohexyl)oxy]dimethylsilane
    3. CAS NO:124414-01-3
    4. Molecular Formula:
    5. Molecular Weight: 274.476
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 124414-01-3.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: tert-butyl[(4,4-dimethoxycyclohexyl)oxy]dimethylsilane(CAS DataBase Reference)
    10. NIST Chemistry Reference: tert-butyl[(4,4-dimethoxycyclohexyl)oxy]dimethylsilane(124414-01-3)
    11. EPA Substance Registry System: tert-butyl[(4,4-dimethoxycyclohexyl)oxy]dimethylsilane(124414-01-3)

  • 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: 124414-01-3(Hazardous Substances Data)

124414-01-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 124414-01-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,4,1 and 4 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 124414-01:
(8*1)+(7*2)+(6*4)+(5*4)+(4*1)+(3*4)+(2*0)+(1*1)=83
83 % 10 = 3
So 124414-01-3 is a valid CAS Registry Number.

124414-01-3Relevant articles and documents

FRET Pairs with Fixed Relative Orientation of Chromophores

Wessig, Pablo,Behrends, Nicole,Kumke, Michael U.,Eisold, Ursula

, p. 4476 - 4486 (2016)

Synthetic routes to different oligospirothioketal (OSTK) F?rster resonance energy transfer (FRET) constructs are described and the photophysics of these constructs were explored in different solvents. The FRET efficiencies were determined from the experim

High-pressure-promoted uncatalyzed ketalization of ketones and oxy-Michael/ketalization of conjugated enones

Kumamoto, Koji,Ichikawa, Yoshiyasu,Kotsuki, Hiyoshizo

, p. 2254 - 2256 (2007/10/03)

A new practical method for ketalization or oxy-Michael/ketalization was developed using the high-pressure-promoted condensation of ketones or α,β-unsaturated ketones with alcohols in the presence of trialkyl orthoformates as water scavengers. Georg Thieme Verlag Stuttgart.

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