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CAS

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172325-07-4

O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl)-L-serine benzyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 172325-07-4 Structure

  • Basic information

    1. Product Name: O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl)-L-serine benzyl ester
    2. Synonyms: O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl)-L-serine benzyl ester
    3. CAS NO:172325-07-4
    4. Molecular Formula:
    5. Molecular Weight: 508.485
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 172325-07-4.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: O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl)-L-serine benzyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl)-L-serine benzyl ester(172325-07-4)
    11. EPA Substance Registry System: O-(3,4,6-tri-O-acetyl-2-azido-2-deoxy-α-D-glucopyranosyl)-L-serine benzyl ester(172325-07-4)

  • 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: 172325-07-4(Hazardous Substances Data)

172325-07-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 172325-07-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,2,3,2 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 172325-07:
(8*1)+(7*7)+(6*2)+(5*3)+(4*2)+(3*5)+(2*0)+(1*7)=114
114 % 10 = 4
So 172325-07-4 is a valid CAS Registry Number.

172325-07-4Upstream product

172325-07-4Relevant articles and documents

Stereoselective synthesis of O-serinyl/threoninyl-2-acetamido-2-deoxy-α- or β-glycosides

Szabo,Ramza,Langdon,Polt

, p. 11 - 28 (2007/10/03)

General glycosidation methodology has been developed which can selectively provide 2-acetamido-2-deoxy-α- or β-glycosides of β-hydroxy-α-amino acid derivatives [glucopyranoside-(8, 43), galactopyranoside- (9, 13), mannopyranoside- (10), lactoside analogs (11, 38) and 3-O-β-galactopyranosyl-mannopyranoside (12)] stereoselectively in excellent yield from the highly nucleophilic α-imino esters (Schiff bases) of L-serine and L-threonine. Various glycosides were converted via their amino and acetamido derivatives to Fmoc-protected serinyl- or threoninyl-glycosides (24-28, 37, 41, 46) which are all suitable building blocks for the solid-phase synthesis of O-glycopeptides. Complete 1H- and 13C-NMR data are provided for all compounds.

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