Cas 333384-36-4,N-((2R,3R,4R,5S,6R)-3-Acetylamino-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-2-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-acetamide

333384-36-4

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Basic information

Product Name: N-((2R,3R,4R,5S,6R)-3-Acetylamino-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-2-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-acetamide
Synonyms:
CAS NO:333384-36-4
Molecular Formula:
Molecular Weight: 357.32
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: N-((2R,3R,4R,5S,6R)-3-Acetylamino-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-2-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-acetamide(CAS DataBase Reference)
NIST Chemistry Reference: N-((2R,3R,4R,5S,6R)-3-Acetylamino-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-2-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-acetamide(333384-36-4)
EPA Substance Registry System: N-((2R,3R,4R,5S,6R)-3-Acetylamino-4,5-dihydroxy-6-hydroxymethyl-tetrahydro-pyran-2-yl)-2-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-acetamide(333384-36-4)

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: 333384-36-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 333384-36-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,3,3,8 and 4 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 333384-36:
(8*3)+(7*3)+(6*3)+(5*3)+(4*8)+(3*4)+(2*3)+(1*6)=134
134 % 10 = 4
So 333384-36-4 is a valid CAS Registry Number.

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333384-36-4Relevant academic research and scientific papers

Chemoselective ligation of maleimidosugars to peptides/protein for the preparation of neoglycopeptides/neoglycoprotein

Shin, Injae,Jung, Hyuk-Jun,Lee, Myung-Ryul

, p. 1325 - 1328 (2007/10/03)

Two types of maleimidosugars as thiol-selective carbohydrates, 1-maleimidosugars and acetyl-linked maleimidosugars, were efficiently synthesized. They were coupled to glutathione, Fas peptide and bovine serium albumin (BSA) to prepare the corresponding glycosylated peptides and a protein via stable thioether linkages in a chemoselective manner.

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