Cas 866416-49-1,N-acetyl-N-(p-methylphenyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)thiourea

866416-49-1

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Basic information

Product Name: N-acetyl-N-(p-methylphenyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)thiourea
Synonyms: N-acetyl-N-(p-methylphenyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)thiourea
CAS NO:866416-49-1
Molecular Formula:
Molecular Weight: 538.576
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-acetyl-N-(p-methylphenyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)thiourea(CAS DataBase Reference)
NIST Chemistry Reference: N-acetyl-N-(p-methylphenyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)thiourea(866416-49-1)
EPA Substance Registry System: N-acetyl-N-(p-methylphenyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)thiourea(866416-49-1)

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: 866416-49-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 866416-49-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,6,4,1 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 866416-49:
(8*8)+(7*6)+(6*6)+(5*4)+(4*1)+(3*6)+(2*4)+(1*9)=201
201 % 10 = 1
So 866416-49-1 is a valid CAS Registry Number.

866416-49-1Upstream product

866416-49-1Downstream Products

105014-62-8 N-(p-methylphenyl)-N'-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)thiourea

866416-49-1Relevant academic research and scientific papers

New synthetic approaches to sugar ureas. Access to ureido-β- cyclodextrins

López, óscar,Maza, Susana,Maya, Inés,Fuentes, José,Fernández-Bola?os, José G.

, p. 9058 - 9069 (2005)

An efficient method for the preparation of urea-bridged cyclodextrins using triphosgene in the isocyanation step in an aqueous two-phase system is reported. Per-O-acetylated glycopyranosylamines and 2-amino-2-deoxy-α and β-d-glucose were also transformed

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