Cas 492448-80-3,3,5-di-O-benzoyl-4-O-(N,N'-dicyclohexylisoureido)-1,2-O-isopropylidene-β-D-fructopyranose

492448-80-3

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Basic information

Product Name: 3,5-di-O-benzoyl-4-O-(N,N'-dicyclohexylisoureido)-1,2-O-isopropylidene-β-D-fructopyranose
Synonyms: 3,5-di-O-benzoyl-4-O-(N,N'-dicyclohexylisoureido)-1,2-O-isopropylidene-β-D-fructopyranose
CAS NO:492448-80-3
Molecular Formula:
Molecular Weight: 634.77
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: 3,5-di-O-benzoyl-4-O-(N,N'-dicyclohexylisoureido)-1,2-O-isopropylidene-β-D-fructopyranose(CAS DataBase Reference)
NIST Chemistry Reference: 3,5-di-O-benzoyl-4-O-(N,N'-dicyclohexylisoureido)-1,2-O-isopropylidene-β-D-fructopyranose(492448-80-3)
EPA Substance Registry System: 3,5-di-O-benzoyl-4-O-(N,N'-dicyclohexylisoureido)-1,2-O-isopropylidene-β-D-fructopyranose(492448-80-3)

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: 492448-80-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 492448-80-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,9,2,4,4 and 8 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 492448-80:
(8*4)+(7*9)+(6*2)+(5*4)+(4*4)+(3*8)+(2*8)+(1*0)=183
183 % 10 = 3
So 492448-80-3 is a valid CAS Registry Number.

492448-80-3Upstream product

538-75-0 dicyclohexyl-carbodiimide

492448-80-3Downstream Products

492448-80-3Relevant academic research and scientific papers

Non-anomeric sugar isoureas

Sowa, Christian,Miethchen, Ralf,Reinke, Helmut

, p. 293 - 303 (2002)

Six non-anomeric isourea derivatives of D-fructose (7, 8), D-glucose (9, 10), 6-deoxy-L-altrose (11) and L-rhamnose (12) were synthesized from the precursors 1-6 by a CuCl-catalyzed addition of a non-glycosidic OH-group to DCC and DIPC, respectively. Subs

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