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CAS

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87265-43-8

N-(3-benzyloxy-4-methoxybenzyl)-2-aminoethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 87265-43-8 Structure

  • Basic information

    1. Product Name: N-(3-benzyloxy-4-methoxybenzyl)-2-aminoethanol
    2. Synonyms:
    3. CAS NO:87265-43-8
    4. Molecular Formula:
    5. Molecular Weight: 287.359
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 87265-43-8.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: N-(3-benzyloxy-4-methoxybenzyl)-2-aminoethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(3-benzyloxy-4-methoxybenzyl)-2-aminoethanol(87265-43-8)
    11. EPA Substance Registry System: N-(3-benzyloxy-4-methoxybenzyl)-2-aminoethanol(87265-43-8)

  • 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: 87265-43-8(Hazardous Substances Data)

87265-43-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 87265-43-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,6 and 5 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87265-43:
(7*8)+(6*7)+(5*2)+(4*6)+(3*5)+(2*4)+(1*3)=158
158 % 10 = 8
So 87265-43-8 is a valid CAS Registry Number.

87265-43-8Relevant articles and documents

A NOVEL ROUTE TO THE SYNTHESIS OF SUBSTITUTED N-BENZYL-1,2,3,4-TETRAHYDROISOQUINOLINES. SYNTHESIS OF SENDAVERINE AND CORGOINE

Masood, M.,Tiwari, K. P.

, p. 177 - 182 (2007/10/02)

The condensation product of 2-aminoethanol with substituted benzaldehyde was reduced and N-benzylated with substituted benzyl chloride followed by PPA cyclization to obtain substituted N-benzyl-tetrahydroisoquinolines; likewise the condensation product of

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