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CAS

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556039-02-2

phenyl 3-O-allyl-4-O-p-methoxybenzyl-1-thio-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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  • 556039-02-2 Structure

  • Basic information

    1. Product Name: phenyl 3-O-allyl-4-O-p-methoxybenzyl-1-thio-β-D-glucopyranoside
    2. Synonyms: phenyl 3-O-allyl-4-O-p-methoxybenzyl-1-thio-β-D-glucopyranoside
    3. CAS NO:556039-02-2
    4. Molecular Formula:
    5. Molecular Weight: 432.538
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 556039-02-2.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: phenyl 3-O-allyl-4-O-p-methoxybenzyl-1-thio-β-D-glucopyranoside(CAS DataBase Reference)
    10. NIST Chemistry Reference: phenyl 3-O-allyl-4-O-p-methoxybenzyl-1-thio-β-D-glucopyranoside(556039-02-2)
    11. EPA Substance Registry System: phenyl 3-O-allyl-4-O-p-methoxybenzyl-1-thio-β-D-glucopyranoside(556039-02-2)

  • 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: 556039-02-2(Hazardous Substances Data)

556039-02-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 556039-02-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,5,6,0,3 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 556039-02:
(8*5)+(7*5)+(6*6)+(5*0)+(4*3)+(3*9)+(2*0)+(1*2)=152
152 % 10 = 2
So 556039-02-2 is a valid CAS Registry Number.

556039-02-2Relevant articles and documents

Carbohydrate-based scaffolds for the generation of sortiments of bioactive compounds

Peri, Francesco,Cipolla, Laura,Forni, Eleonora,Nicotra, Francesco

, p. 369 - 382 (2002)

The polyfunctionality and conformational rigidity of carbohydrates make this class of compounds ideal scaffolds for the production of sortiments1 of bioactive compounds. Examples of carbohydrate-derived peptidomimetics of biological interest, such as somatostatin agonists and integrin antagonists, are presented. In order to have access to solid phase supported sortiments of compounds, orthogonally protected or unprotected carbohydrates were linked to polymers and reacted in the solid phase employing different regioselective strategies. Original bicyclic and tricyclic glycidic scaffolds were easily obtained starting from natural sugars such as D-arabinose and D-fructose. Manipulation of these conformationally blocked compounds afforded different carbohydrate-based derivatives, among which azidoacids are useful precursors of β-turn peptidomimetics.

D-glucose as a regioselectively addressable scaffold for combinatorial chemistry on solid phase

Peri, Francesco,Nicotra, Francesco,Leslie, Colin P.,Micheli, Fabrizio,Seneci, Pierfausto,Marchioro, Carla

, p. 57 - 71 (2007/10/03)

D-Glucose derivatives bearing an anomeric thiophenyl group and orthogonally protections on secondary hydroxyl groups were linked to solid supports (PS/DV polymer, tentagel resin) through an ester bond on C-6. It was investigated the possibility to remove orthogonally protecting groups and functionalize selectively the free hydroxyls groups and the anomeric carbon of sugars in solid phase.

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