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CAS

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121377-24-0

2-(trimethylsilyl)ethyl 3-O-benzoyl-β-D-galactopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 121377-24-0 Structure

  • Basic information

    1. Product Name: 2-(trimethylsilyl)ethyl 3-O-benzoyl-β-D-galactopyranoside
    2. Synonyms: 2-(trimethylsilyl)ethyl 3-O-benzoyl-β-D-galactopyranoside
    3. CAS NO:121377-24-0
    4. Molecular Formula:
    5. Molecular Weight: 384.502
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 121377-24-0.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-(trimethylsilyl)ethyl 3-O-benzoyl-β-D-galactopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(trimethylsilyl)ethyl 3-O-benzoyl-β-D-galactopyranoside(121377-24-0)
    11. EPA Substance Registry System: 2-(trimethylsilyl)ethyl 3-O-benzoyl-β-D-galactopyranoside(121377-24-0)

  • 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: 121377-24-0(Hazardous Substances Data)

121377-24-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 121377-24-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,1,3,7 and 7 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 121377-24:
(8*1)+(7*2)+(6*1)+(5*3)+(4*7)+(3*7)+(2*2)+(1*4)=100
100 % 10 = 0
So 121377-24-0 is a valid CAS Registry Number.

121377-24-0Relevant articles and documents

Process for producing sialic acid derivatives

-

, (2008/06/13)

The present invention provides a process for selective production of a 2-α-O-glycoside compound of sialic acid which is useful as a starting material or intermediate for medicines and biochemical reagents. The process comprises reacting an alkylthiosialic acid derivative represented by the formula [I]: STR1 wherein R represents an acyl group and R1 and R2 each represents a lower alkyl group with a compound having alcoholic hydroxyl group at a low temperature in a polar solvent having no hydroxyl group in the presence of a Lewis acid selected from the group consisting of methyl triflate, trimethylsilyl triflate and dimethyl(methylthio)sulfonium triflate. The present invention further provides novel compounds.

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