Cas 1352575-76-8,benzyl 5-uracil-1-yl-pentyl 3-(2-acetamido-b-2-deoxy-α-D-glucopyranosyl)-2-oxopropylphosphonate

1352575-76-8

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Basic information

Product Name: benzyl 5-uracil-1-yl-pentyl 3-(2-acetamido-b-2-deoxy-α-D-glucopyranosyl)-2-oxopropylphosphonate
Synonyms: benzyl 5-uracil-1-yl-pentyl 3-(2-acetamido-b-2-deoxy-α-D-glucopyranosyl)-2-oxopropylphosphonate
CAS NO:1352575-76-8
Molecular Formula:
Molecular Weight: 611.586
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: benzyl 5-uracil-1-yl-pentyl 3-(2-acetamido-b-2-deoxy-α-D-glucopyranosyl)-2-oxopropylphosphonate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 5-uracil-1-yl-pentyl 3-(2-acetamido-b-2-deoxy-α-D-glucopyranosyl)-2-oxopropylphosphonate(1352575-76-8)
EPA Substance Registry System: benzyl 5-uracil-1-yl-pentyl 3-(2-acetamido-b-2-deoxy-α-D-glucopyranosyl)-2-oxopropylphosphonate(1352575-76-8)

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: 1352575-76-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1352575-76-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,2,5,7 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1352575-76:
(9*1)+(8*3)+(7*5)+(6*2)+(5*5)+(4*7)+(3*5)+(2*7)+(1*6)=168
168 % 10 = 8
So 1352575-76-8 is a valid CAS Registry Number.

1352575-76-8Upstream product

1352575-74-6 benzyl 5-(3-N-tert-butyloxycarbonyl-uracil-1-yl)pentyl-3-(2-acetamido-4,6-O-(R)-benzylidene-3-O-tertbutyldimethylsilyl-2-deoxy-α-D-glucopyranosyl)-2-oxopropylphosphonate

1352575-76-8Downstream Products

1352575-76-8Relevant academic research and scientific papers

Synthesis and biological evaluation of potential new inhibitors of the bacterial transferase MraY with a β-ketophosphonate structure

Auberger, Nicolas,Frlan, Rok,Al-Dabbagh, Bayan,Bouhss, Ahmed,Crouvoisier, Muriel,Gravier-Pelletier, Christine,Merrer, Yves Le

, p. 8301 - 8312 (2011)

Stable analogs of bacterial transferase MraY substrate or product with a pyrophosphate surrogate in their structure are described. β- ketophosphonates were designed as pyrophosphate bioisosteres and were investigated as UDP-GlcNAc mimics. The developed st

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