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162283-20-7

Quinoline, 2-methyl-4-[(trimethylsilyl)oxy]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 162283-20-7 Structure

  • Basic information

    1. Product Name: Quinoline, 2-methyl-4-[(trimethylsilyl)oxy]- (9CI)
    2. Synonyms: Quinoline, 2-methyl-4-[(trimethylsilyl)oxy]- (9CI)
    3. CAS NO:162283-20-7
    4. Molecular Formula: C13H17NOSi
    5. Molecular Weight: 231.36568
    6. EINECS: N/A
    7. Product Categories: SILYL
    8. Mol File: 162283-20-7.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 297.1±20.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.024±0.06 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 6.43±0.50(Predicted)
    10. CAS DataBase Reference: Quinoline, 2-methyl-4-[(trimethylsilyl)oxy]- (9CI)(CAS DataBase Reference)
    11. NIST Chemistry Reference: Quinoline, 2-methyl-4-[(trimethylsilyl)oxy]- (9CI)(162283-20-7)
    12. EPA Substance Registry System: Quinoline, 2-methyl-4-[(trimethylsilyl)oxy]- (9CI)(162283-20-7)

  • 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: 162283-20-7(Hazardous Substances Data)

162283-20-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 162283-20-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,2,2,8 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 162283-20:
(8*1)+(7*6)+(6*2)+(5*2)+(4*8)+(3*3)+(2*2)+(1*0)=117
117 % 10 = 7
So 162283-20-7 is a valid CAS Registry Number.

162283-20-7Downstream Products

162283-20-7Relevant articles and documents

A type II polyketide synthase from the gram-negative bacterium Stigmatella aurantiaca is involved in aurachin alkaloid biosynthesis

Sandmann, Axel,Dickschat, Jeroen,Jenke-Kodama, Holger,Kunze, Brigitte,Dittmann, Elke,Mueller, Rolf

, p. 2712 - 2716 (2007)

A closer look: The path for the biosynthesis of aurachin alkaloids (aurachin A is shown) has been deduced by molecular biological methods, including the cloning and sequencing of the biosynthetic gene cluster in the bacterium Stigmatella aurantiaca. The gene cluster encodes a type II polyketide synthase, which was discovered in this form for the first time in a Gram-negative bacterium. (Chemical Equation Presented).

Alkylation of 2-, 4-, and 8-Trialkylsiloxyquinolines by Methyl Iodide

Lukevits, E.,Segal, I.,Birgele, I.,Zablotskaya, A.

, p. 1061 - 1066 (2007/10/03)

Trimethyl- and triethylsilyl ethers of 2-, 4-, and 8-hydroxyquinolines have been prepared.The alkylation of these siloxyquinolines by methyl iodide has been studied.In the case of 4-trimethylsiloxyquinaldine, it has been established that both N- and O-alkylation products are formed.

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