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CAS

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83585-51-7

(1,4,7,10,13-Pentaoxa-cyclopentadec-2-ylmethyl)-phenyl-amine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83585-51-7 Structure

  • Basic information

    1. Product Name: (1,4,7,10,13-Pentaoxa-cyclopentadec-2-ylmethyl)-phenyl-amine
    2. Synonyms: (1,4,7,10,13-Pentaoxa-cyclopentadec-2-ylmethyl)-phenyl-amine
    3. CAS NO:83585-51-7
    4. Molecular Formula:
    5. Molecular Weight: 325.405
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83585-51-7.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: (1,4,7,10,13-Pentaoxa-cyclopentadec-2-ylmethyl)-phenyl-amine(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1,4,7,10,13-Pentaoxa-cyclopentadec-2-ylmethyl)-phenyl-amine(83585-51-7)
    11. EPA Substance Registry System: (1,4,7,10,13-Pentaoxa-cyclopentadec-2-ylmethyl)-phenyl-amine(83585-51-7)

  • 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: 83585-51-7(Hazardous Substances Data)

83585-51-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83585-51-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,8 and 5 respectively; the second part has 2 digits, 5 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 83585-51:
(7*8)+(6*3)+(5*5)+(4*8)+(3*5)+(2*5)+(1*1)=157
157 % 10 = 7
So 83585-51-7 is a valid CAS Registry Number.

83585-51-7Downstream Products

83585-51-7Relevant articles and documents

Synthesis of Aminomethyl Crown Ethers

Maeda, Hirokazu,Kikui, Takashi,Nakatsuji, Yohji,Okahara, Mitsuo

, p. 5167 - 5171 (2007/10/02)

Various N-substituted or unsubstituted aminomethyl crown ethers, which possess a reactive amino group, were prepared in good yields by the reaction between 3-amino-1,2-propanediols or aminomethyl oligoethylene glycols and oligoethylene glycol ditosylates or dichlorides.The scope of the reaction was investigated and the complexing ability of these new crown ether derivatives with sodium and potassium ions in methanol was measured by potentiometric titration.

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