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CAS

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851445-36-8

2-(allyloxycarbonylamino)ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-(allyloxycarbonylamino)-β-D-glucopyranoside is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 851445-36-8 Structure

  • Basic information

    1. Product Name: 2-(allyloxycarbonylamino)ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-(allyloxycarbonylamino)-β-D-glucopyranoside
    2. Synonyms:
    3. CAS NO:851445-36-8
    4. Molecular Formula:
    5. Molecular Weight: 516.502
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 851445-36-8.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: 2-(allyloxycarbonylamino)ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-(allyloxycarbonylamino)-β-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(allyloxycarbonylamino)ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-(allyloxycarbonylamino)-β-D-glucopyranoside(851445-36-8)
    11. EPA Substance Registry System: 2-(allyloxycarbonylamino)ethyl 3,4,6-tri-O-acetyl-2-deoxy-2-(allyloxycarbonylamino)-β-D-glucopyranoside(851445-36-8)

  • 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: 851445-36-8(Hazardous Substances Data)

851445-36-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 851445-36-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,5,1,4,4 and 5 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 851445-36:
(8*8)+(7*5)+(6*1)+(5*4)+(4*4)+(3*5)+(2*3)+(1*6)=168
168 % 10 = 8
So 851445-36-8 is a valid CAS Registry Number.

851445-36-8Downstream Products

851445-36-8Relevant articles and documents

New synthesis of glycolipid immunostimulants RC-529 and CRX-524

Bazin, Hélène G.,Bess, Laura S.,Livesay, Mark T.,Ryter, Kendal T.,Johnson, Craig L.,Arnold, Jeffrey S.,Johnson, David A.

, p. 2087 - 2092 (2006)

An efficient and scalable synthesis of the potent vaccine adjuvant RC-529 (3) and TLR4 agonist CRX-524 (4) is described in eight steps from 1,3,4,6-tetra-O-acetyl-2-amino-2-benzyloxycarbonyl-2-deoxy-β-d- glucopyranose (10c) in ca. 25% overall yield. The synthesis features the strategic use of the N-Cbz group for β-glycosylation and the selective N,N,O-triacylation of common advanced intermediate 15 with (R)-3- tetradecanoyloxy or decanoyloxytetradecanoic acid (8, 9) late in the synthesis. A new method for preparing and enhancing the enantiopurity of (R)-3-hydroxytetradecanoic acid (6), a key component of 3 and 4 as well as bacterial lipid A, is also described.

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