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220869-68-1

2-benzamido-2-deoxy-1-O-t-butyldiphenylsilyl-4,6-O-ethylidene-3-O-methylsulfonyl-D-glucitol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 220869-68-1 Structure

  • Basic information

    1. Product Name: 2-benzamido-2-deoxy-1-O-t-butyldiphenylsilyl-4,6-O-ethylidene-3-O-methylsulfonyl-D-glucitol
    2. Synonyms: 2-benzamido-2-deoxy-1-O-t-butyldiphenylsilyl-4,6-O-ethylidene-3-O-methylsulfonyl-D-glucitol
    3. CAS NO:220869-68-1
    4. Molecular Formula:
    5. Molecular Weight: 627.831
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 220869-68-1.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: 2-benzamido-2-deoxy-1-O-t-butyldiphenylsilyl-4,6-O-ethylidene-3-O-methylsulfonyl-D-glucitol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzamido-2-deoxy-1-O-t-butyldiphenylsilyl-4,6-O-ethylidene-3-O-methylsulfonyl-D-glucitol(220869-68-1)
    11. EPA Substance Registry System: 2-benzamido-2-deoxy-1-O-t-butyldiphenylsilyl-4,6-O-ethylidene-3-O-methylsulfonyl-D-glucitol(220869-68-1)

  • 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: 220869-68-1(Hazardous Substances Data)

220869-68-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 220869-68-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,0,8,6 and 9 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 220869-68:
(8*2)+(7*2)+(6*0)+(5*8)+(4*6)+(3*9)+(2*6)+(1*8)=141
141 % 10 = 1
So 220869-68-1 is a valid CAS Registry Number.

220869-68-1Relevant articles and documents

Stereocontrolled synthesis of novel phytosphingosine-type glucosaminocerebrosides

Murakami, Teiichi,Taguchi, Kazuhiro

, p. 989 - 1004 (1999)

D-ribo-Phytosphingosine 1 was conveniently synthesized from N-benzoyl- D-glucosamine 3 by an improved route in which regioselective O- methanesulfonation and diastereoselective Grignard addition are involved as key steps. Using a synthetic intermediate of 1, novel D-ribo- phytosphingosine-type glycolipids 2a and 2b, unnatural homologues of antifungal cerebrosides Halicylindrosides, were efficiently synthesized in a stereocontrolled manner.

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