Cas 285560-53-4,1-(6-O-acetyl-4-O-cyclohexylcarbamoyl-2,3-O-ethylidene-β-D-gulopyranosyl)-5-trifluoromethyl-4-phenyl-1,2,3-triazole

285560-53-4

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Basic information

Product Name: 1-(6-O-acetyl-4-O-cyclohexylcarbamoyl-2,3-O-ethylidene-β-D-gulopyranosyl)-5-trifluoromethyl-4-phenyl-1,2,3-triazole
Synonyms: 1-(6-O-acetyl-4-O-cyclohexylcarbamoyl-2,3-O-ethylidene-β-D-gulopyranosyl)-5-trifluoromethyl-4-phenyl-1,2,3-triazole
CAS NO:285560-53-4
Molecular Formula:
Molecular Weight: 568.55
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: 1-(6-O-acetyl-4-O-cyclohexylcarbamoyl-2,3-O-ethylidene-β-D-gulopyranosyl)-5-trifluoromethyl-4-phenyl-1,2,3-triazole(CAS DataBase Reference)
NIST Chemistry Reference: 1-(6-O-acetyl-4-O-cyclohexylcarbamoyl-2,3-O-ethylidene-β-D-gulopyranosyl)-5-trifluoromethyl-4-phenyl-1,2,3-triazole(285560-53-4)
EPA Substance Registry System: 1-(6-O-acetyl-4-O-cyclohexylcarbamoyl-2,3-O-ethylidene-β-D-gulopyranosyl)-5-trifluoromethyl-4-phenyl-1,2,3-triazole(285560-53-4)

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: 285560-53-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 285560-53-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,8,5,5,6 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 285560-53:
(8*2)+(7*8)+(6*5)+(5*5)+(4*6)+(3*0)+(2*5)+(1*3)=164
164 % 10 = 4
So 285560-53-4 is a valid CAS Registry Number.

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285560-53-4Relevant academic research and scientific papers

Organofluorine compounds and fluorinating agents. 27: New trifluoromethyl substituted 1,2,3-triazoles linked to D-galactose and D-gulose

Hager, Christian,Miethchen, Ralf,Reinke, Helmut

, p. 414 - 420 (2007/10/03)

The title compounds were synthesized by 1,3-dipolar cycloaddition of 3,3,3-trifluoropropinyl benzene (2) to the azido sugars 2,3,4,6-tetra-O-acetyl-β-D-galactopyranosyl azide (1), 6-O-acetyl-4-O-cyclohexylcarbamoyl-2,3-O-(2,2,2-trichloroethylidene)-β-D- g

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