Cas 179092-63-8,Nα-(9-fluorenylmethoxycarbonyl)-3-O-[(2,3,6-tri-O-acetyl)-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-β-D-glucopyranosyl]-L-serine

179092-63-8

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Basic information

Product Name: Nα-(9-fluorenylmethoxycarbonyl)-3-O-[(2,3,6-tri-O-acetyl)-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-β-D-glucopyranosyl]-L-serine
Synonyms: Nα-(9-fluorenylmethoxycarbonyl)-3-O-[(2,3,6-tri-O-acetyl)-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-β-D-glucopyranosyl]-L-serine
CAS NO:179092-63-8
Molecular Formula:
Molecular Weight: 945.882
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: Nα-(9-fluorenylmethoxycarbonyl)-3-O-[(2,3,6-tri-O-acetyl)-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-β-D-glucopyranosyl]-L-serine(CAS DataBase Reference)
NIST Chemistry Reference: Nα-(9-fluorenylmethoxycarbonyl)-3-O-[(2,3,6-tri-O-acetyl)-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-β-D-glucopyranosyl]-L-serine(179092-63-8)
EPA Substance Registry System: Nα-(9-fluorenylmethoxycarbonyl)-3-O-[(2,3,6-tri-O-acetyl)-4-O-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-β-D-glucopyranosyl]-L-serine(179092-63-8)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 179092-63-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 179092-63-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,7,9,0,9 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 179092-63:
(8*1)+(7*7)+(6*9)+(5*0)+(4*9)+(3*2)+(2*6)+(1*3)=168
168 % 10 = 8
So 179092-63-8 is a valid CAS Registry Number.

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179092-63-8Relevant academic research and scientific papers

Facile synthesis of glycosylated Fmoc amino acid building blocks assisted by microwave irradiation

Yao, Nianhuan,Fung, Gabriel,Malekan, Hamed,Ye, Long,Kurth, Mark J.,Lam, Kit S.

, p. 2277 - 2281 (2010)

The synthesis of glycosylated Fmoc amino acids by reaction of mono- and disaccharide peracetates with Fmoc amino acids having free carboxyl groups was rapidly promoted by Lewis acids (SnCl4, BF3·Et 2O) under microwave irradiation. The products are useful building blocks for the synthesis of glycopeptides.

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