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1037195-49-5

(2-O-arachidyl-1-O-stearyl-sn-glycer-3-yl) (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl) phosphate triethylammonium salt is a complex organic molecule with a glycerol backbone, a phospholipid, and a glucopyranosyl group. The molecule has a negatively charged phosphate group and a positively charged triethylammonium salt counterion. The acetyl groups on the glucopyranosyl group contribute to the overall structure and properties of the compound.

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  • 1037195-49-5 Structure

  • Basic information

    1. Product Name: (2-O-arachidyl-1-O-stearyl-sn-glycer-3-yl) (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl) phosphate triethylammonium salt
    2. Synonyms:
    3. CAS NO:1037195-49-5
    4. Molecular Formula:
    5. Molecular Weight: 1164.55
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1037195-49-5.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-O-arachidyl-1-O-stearyl-sn-glycer-3-yl) (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl) phosphate triethylammonium salt(CAS DataBase Reference)
    10. NIST Chemistry Reference: (2-O-arachidyl-1-O-stearyl-sn-glycer-3-yl) (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl) phosphate triethylammonium salt(1037195-49-5)
    11. EPA Substance Registry System: (2-O-arachidyl-1-O-stearyl-sn-glycer-3-yl) (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl) phosphate triethylammonium salt(1037195-49-5)

  • 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: 1037195-49-5(Hazardous Substances Data)

1037195-49-5 Usage

Uses

Used in Pharmaceutical Applications:
(2-O-arachidyl-1-O-stearyl-sn-glycer-3-yl) (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl) phosphate triethylammonium salt is used as a potential pharmaceutical agent for [application reason]. The specific application reason is not provided in the materials.
Used in Biotechnology Applications:
(2-O-arachidyl-1-O-stearyl-sn-glycer-3-yl) (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl) phosphate triethylammonium salt is used as a potential biotechnology agent for [application reason]. The specific application reason is not provided in the materials.
Note: The specific application reasons for the pharmaceutical and biotechnology uses are not provided in the materials. Further research and testing would be necessary to determine the specific uses and properties of (2-O-arachidyl-1-O-stearyl-sn-glycer-3-yl) (2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl) phosphate triethylammonium salt.

Check Digit Verification of cas no

The CAS Registry Mumber 1037195-49-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,7,1,9 and 5 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1037195-49:
(9*1)+(8*0)+(7*3)+(6*7)+(5*1)+(4*9)+(3*5)+(2*4)+(1*9)=145
145 % 10 = 5
So 1037195-49-5 is a valid CAS Registry Number.

1037195-49-5 Well-known Company Product Price

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  • TCI America

  • (P2079)  2,3,4,6-Tetra-O-acetyl-PtdGlc(di-acyl Chain)  

  • 1037195-49-5

  • 0.00CNY

  • Detail

1037195-49-5Downstream Products

1037195-49-5Relevant articles and documents

First synthesis of natural phosphatidyl-β-d-glucoside

Greimel, Peter,Ito, Yukishige

, p. 3562 - 3566 (2008/09/19)

Herein, we report the chemical synthesis of naturally occurring mammalian phosphatidyl-β-d-glucoside (PtdGlc), in order to confirm the proposed structure and to clarify its stereochemistry. We designed a convergent synthetic strategy, suitable to prepare

Syntheses of phosphatidyl-β-d-glucoside analogues to probe antigen selectivity of monoclonal antibody 'DIM21'

Greimel, Peter,Lapeyre, Milaine,Nagatsuka, Yasuko,Hirabayashi, Yoshio,Ito, Yukishige

, p. 7210 - 7217 (2008/12/23)

Herein, we report the chemical syntheses of a series of phosphatidyl-β-d-glucoside (PtdGlc) analogues, including 6-O-Ac, sn-2-O-Me, phosphorothioate as well as phosphatidylgalactoside and -mannoside derivatives. In the key step, β-glycosyl H-phosphonate w

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