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215869-20-8

(1S,2S,3S,4R,5R,6S)-2,3,4,5-Tetrakis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 215869-20-8 Structure

  • Basic information

    1. Product Name: (1S,2S,3S,4R,5R,6S)-2,3,4,5-Tetrakis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexanol
    2. Synonyms:
    3. CAS NO:215869-20-8
    4. Molecular Formula:
    5. Molecular Weight: 660.807
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 215869-20-8.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: (1S,2S,3S,4R,5R,6S)-2,3,4,5-Tetrakis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: (1S,2S,3S,4R,5R,6S)-2,3,4,5-Tetrakis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexanol(215869-20-8)
    11. EPA Substance Registry System: (1S,2S,3S,4R,5R,6S)-2,3,4,5-Tetrakis-benzyloxy-6-(4-methoxy-benzyloxy)-cyclohexanol(215869-20-8)

  • 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: 215869-20-8(Hazardous Substances Data)

215869-20-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 215869-20-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,5,8,6 and 9 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 215869-20:
(8*2)+(7*1)+(6*5)+(5*8)+(4*6)+(3*9)+(2*2)+(1*0)=148
148 % 10 = 8
So 215869-20-8 is a valid CAS Registry Number.

215869-20-8Relevant articles and documents

Synthesis of a jojoba bean disaccharide

Kornienko, Alexander,Marnera, Georgia,D'Alarcao, Marc

, p. 141 - 144 (1998)

A synthesis of the disaccharide recently isolated from jojoba beans, 2-O-α-D-galactopyranosyl-D-chiro-inositol, has been achieved. The suitably protected chiro-inositol unit was prepared by an enantiospecific synthesis from L-xylose utilizing SmI2-mediated pinacol coupling as a key step. Copyright (C) 1998 Elsevier Science Ltd.

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