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118358-79-5

N-Fmoc-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-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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  • N-Fmoc-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-L-serine benzyl ester

    Cas No: 118358-79-5

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  • 118358-79-5 Structure

  • Basic information

    1. Product Name: N-Fmoc-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-L-serine benzyl ester
    2. Synonyms: N-Fmoc-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-L-serine benzyl ester
    3. CAS NO:118358-79-5
    4. Molecular Formula:
    5. Molecular Weight: 747.753
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 118358-79-5.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: N-Fmoc-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-L-serine benzyl ester(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-Fmoc-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-L-serine benzyl ester(118358-79-5)
    11. EPA Substance Registry System: N-Fmoc-O-(2,3,4,6-tetra-O-acetyl-α-D-mannopyranosyl)-L-serine benzyl ester(118358-79-5)

  • 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: 118358-79-5(Hazardous Substances Data)

118358-79-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 118358-79-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,5 and 8 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 118358-79:
(8*1)+(7*1)+(6*8)+(5*3)+(4*5)+(3*8)+(2*7)+(1*9)=145
145 % 10 = 5
So 118358-79-5 is a valid CAS Registry Number.

118358-79-5Relevant articles and documents

From solution phase to "on-column" chemistry: Trichloroacetimidate-based glycosylation promoted by perchloric acid-silica

Mukhopadhyay, Balaram,Maurer, Sarah V.,Rudolph, Nadine,Van Well, Renate M.,Russell, David A.,Field, Robert A.

, p. 9059 - 9062 (2005)

Activation of ester-protected glycosyl trichloroacetimidate donors by perchloric acid immobilized on silica afforded 1,2-trans disaccharides in 60-90% yields. Applying this approach to one-pot sequential glycosylation resulted in efficient syntheses of th

Glycosylation of Fmoc amino acids: Preparation of mono- and di-glycosylated derivatives and their incorporation into Arg-Gly-Asp (RGD)-containing glycopeptides

Vegad, Hiran,Gray, Charles J.,Somers, Peter J.,Dutta, Anand S.

, p. 1429 - 1441 (2007/10/03)

Compounds containing O-glycosidic linkages between carbohydrate species (D-glucopyranose, D-mannopyranose and L-rhamnopyranose) and hydroxy-containing amino acid components (L-threonine, L-serine and L-hydroxyproline) have been synthesized. Significant qu

Synthesis and conformational and NMR studies of α-D-mannopyranosyl and α-D-mannopyranosyl-(1-->2)-α-D-mannopyranosyl linked to L-serine and L-threonine

Helander, Anne,Kenne, Lennart,Oscarson, Stefan,Peters, Thomas,Brisson, Jean-Robert

, p. 299 - 318 (2007/10/02)

α-D-Mannopyranosyl and α-D-mannopyranosyl-(1-->2)-α-D-mannopyranosyl linked to L-serine and L-threonine have been synthesised as model substances for the linkage region in certain O-linked glycoproteins.Metropolis Monte Carlo simulations were performed wi

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