Cas 213401-64-0,Acetic acid (2R,3S,4R,5R,6R)-2-acetoxymethyl-5-acetylamino-6-allyloxy-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-4-yl ester

213401-64-0

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Basic information

Product Name: Acetic acid (2R,3S,4R,5R,6R)-2-acetoxymethyl-5-acetylamino-6-allyloxy-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-4-yl ester
Synonyms:
CAS NO:213401-64-0
Molecular Formula:
Molecular Weight: 465.5
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: Acetic acid (2R,3S,4R,5R,6R)-2-acetoxymethyl-5-acetylamino-6-allyloxy-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-4-yl ester(CAS DataBase Reference)
NIST Chemistry Reference: Acetic acid (2R,3S,4R,5R,6R)-2-acetoxymethyl-5-acetylamino-6-allyloxy-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-4-yl ester(213401-64-0)
EPA Substance Registry System: Acetic acid (2R,3S,4R,5R,6R)-2-acetoxymethyl-5-acetylamino-6-allyloxy-3-(4-methoxy-benzyloxy)-tetrahydro-pyran-4-yl ester(213401-64-0)

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: 213401-64-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 213401-64-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,3,4,0 and 1 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 213401-64:
(8*2)+(7*1)+(6*3)+(5*4)+(4*0)+(3*1)+(2*6)+(1*4)=80
80 % 10 = 0
So 213401-64-0 is a valid CAS Registry Number.

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213401-64-0Downstream Products

213401-64-0Relevant academic research and scientific papers

Synthesis of a neoglycoprotein containing the Lewis X analogous trisaccharide β-D-GalpNAc-(1 →4)[α-L-Fucp-(1→3)]-β-D-GlcpNAc

Bartek, Johannes,Mueller, Renate,Kosma, Paul

, p. 259 - 273 (2007/10/03)

The trisaccharide allyl glycoside 36 and related disaccharide part structures have been prepared using the 2-trichloroacetamido-2-deoxy-α-D-galactopyranosyl trichloroacetimidate derivative 9 as glycosyl donor under promotion with TMSOTf or Sn(OTf)2/

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