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CAS

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226919-64-8

dibutyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-galactopyranoside phosphate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 226919-64-8 Structure

  • Basic information

    1. Product Name: dibutyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-galactopyranoside phosphate
    2. Synonyms: dibutyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-galactopyranoside phosphate
    3. CAS NO:226919-64-8
    4. Molecular Formula:
    5. Molecular Weight: 726.844
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 226919-64-8.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: dibutyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-galactopyranoside phosphate(CAS DataBase Reference)
    10. NIST Chemistry Reference: dibutyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-galactopyranoside phosphate(226919-64-8)
    11. EPA Substance Registry System: dibutyl 2-O-pivaloyl-3,4,6-tri-O-benzyl-β-D-galactopyranoside phosphate(226919-64-8)

  • 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: 226919-64-8(Hazardous Substances Data)

226919-64-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 226919-64-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,2,6,9,1 and 9 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 226919-64:
(8*2)+(7*2)+(6*6)+(5*9)+(4*1)+(3*9)+(2*6)+(1*4)=158
158 % 10 = 8
So 226919-64-8 is a valid CAS Registry Number.

226919-64-8Relevant articles and documents

Synthesis of oligosaccharides, reagents and methods related thereto

-

, (2008/06/13)

One aspect of the present invention relates to differentially protected glycosyl phosphates. Another aspect of the present invention relates to the preparation of glycosyl phosphates from glycal precursors. In another aspect of the present invention, glycosyl phosphates are used as glycosyl donors in glycosylation reactions.

Oligosaccharide synthesis with glycosyl phosphate and dithiophosphate triesters as glycosylating agents

Plante,Palmacci,Andrade,Seeberger

, p. 9545 - 9554 (2007/10/03)

Described is an efficient one-pot synthesis of α- and β-glycosyl phosphate and dithiophosphate triesters from glycals via 1,2-anhydrosugars. Glycosyl phosphates function as versatile glycosylating agents for the synthesis of β-glucosidic, β-galactosidic,

Synthesis and use of glycosyl phosphates as glycosyl donors.

Plante,Andrade,Seeberger

, p. 211 - 214 (2008/02/11)

Differentially protected glycosyl phosphates prepared by a straightforward synthesis from glycal precursors are used as powerful glycosyl donors. Activation of beta-glycosyl phosphates by TMSOTf at -78 degrees C achieves the selective formation of beta-gl

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