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CAS

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1587709-89-4

4-(6-(methoxymethoxy)quinolin-2-yl)-N,N-dimethylaniline is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1587709-89-4 Structure

  • Basic information

    1. Product Name: 4-(6-(methoxymethoxy)quinolin-2-yl)-N,N-dimethylaniline
    2. Synonyms: 4-(6-(methoxymethoxy)quinolin-2-yl)-N,N-dimethylaniline
    3. CAS NO:1587709-89-4
    4. Molecular Formula:
    5. Molecular Weight: 308.38
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1587709-89-4.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-(6-(methoxymethoxy)quinolin-2-yl)-N,N-dimethylaniline(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4-(6-(methoxymethoxy)quinolin-2-yl)-N,N-dimethylaniline(1587709-89-4)
    11. EPA Substance Registry System: 4-(6-(methoxymethoxy)quinolin-2-yl)-N,N-dimethylaniline(1587709-89-4)

  • 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: 1587709-89-4(Hazardous Substances Data)

1587709-89-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1587709-89-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,7,7,0 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1587709-89:
(9*1)+(8*5)+(7*8)+(6*7)+(5*7)+(4*0)+(3*9)+(2*8)+(1*9)=234
234 % 10 = 4
So 1587709-89-4 is a valid CAS Registry Number.

1587709-89-4Relevant articles and documents

Enantioselective radiosynthesis of positron emission tomography (PET) tracers containing [18F]fluorohydrins

Graham, Thomas J. A.,Lambert, R. Frederick,Ploessl, Karl,Kung, Hank F.,Doyle, Abigail G.

supporting information, p. 5291 - 5294 (2014/05/06)

Herein, we describe an operationally straightforward radiosynthesis of a chiral transition metal fluoride catalyst, [18F](salen)CoF, and its use for late-stage enantioselective aliphatic radiofluorination. We demonstrate the utility of the method by preparing single enantiomer experimental and clinically validated PET tracers that contain base-sensitive functional groups, epimerizable stereocenters, and nitrogen-rich motifs. Unlike the conventional radiosyntheses of these targets with [18F]KF, labeling with (salen)CoF is possible in the last step and under exceptionally mild conditions. These results constitute a rare example of a nucleophilic radiofluorination using a transition metal fluoride and highlight the potential of such reagents to enhance traditional methods for labeling aliphatic hydrocarbons.

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