Cas 290301-28-9,(R)-2-tert-Butoxycarbonylamino-3-((2S,3R,4R,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-ylsulfanyl)-propionic acid benzyl ester

290301-28-9

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Basic information

Product Name: (R)-2-tert-Butoxycarbonylamino-3-((2S,3R,4R,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-ylsulfanyl)-propionic acid benzyl ester
Synonyms: (R)-2-tert-Butoxycarbonylamino-3-((2S,3R,4R,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-ylsulfanyl)-propionic acid benzyl ester
CAS NO:290301-28-9
Molecular Formula:
Molecular Weight: 640.709
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: (R)-2-tert-Butoxycarbonylamino-3-((2S,3R,4R,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-ylsulfanyl)-propionic acid benzyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (R)-2-tert-Butoxycarbonylamino-3-((2S,3R,4R,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-ylsulfanyl)-propionic acid benzyl ester(290301-28-9)
EPA Substance Registry System: (R)-2-tert-Butoxycarbonylamino-3-((2S,3R,4R,5S,6R)-4,5-diacetoxy-6-acetoxymethyl-3-acetylamino-tetrahydro-pyran-2-ylsulfanyl)-propionic acid benzyl ester(290301-28-9)

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: 290301-28-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 290301-28-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,9,0,3,0 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 290301-28:
(8*2)+(7*9)+(6*0)+(5*3)+(4*0)+(3*1)+(2*2)+(1*8)=109
109 % 10 = 9
So 290301-28-9 is a valid CAS Registry Number.

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290301-28-9Relevant academic research and scientific papers

Facile synthesis of N-Fmoc-serine-S-GlcNAc: A potential molecular probe for the functional study of O-GlcNAc

Ohnishi, Yuki,Ichikawa, Mie,Ichikawa, Yoshitaka

, p. 1289 - 1291 (2000)

A methabolically stable β-N-acetylglucosaminyl-l-thio-N-Fmoc-serine (S-GlcNAc-Ser) derivative was synthesized in two procedures: one involving a coupling of a readily obtainable l-psuedo-thiourea of GlcNAc (S-GlcNAc) and iodo-N-Boc-L-alanine benzyl ester, and the other utilizing a modified Mitsunobu reaction of GlcNAc-SH and a serine derivative. (C) 2000 Elsevier Science Ltd. All rights reserved.

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