Cas 250235-52-0,(R)-5-O-cyclohexylcarbamoyl-1,2-O-isopropylidene-3,4-O-(2,2,2-trichloroethylidene)-β-D-tagatopyranose

250235-52-0

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Basic information

Product Name: (R)-5-O-cyclohexylcarbamoyl-1,2-O-isopropylidene-3,4-O-(2,2,2-trichloroethylidene)-β-D-tagatopyranose
Synonyms: (R)-5-O-cyclohexylcarbamoyl-1,2-O-isopropylidene-3,4-O-(2,2,2-trichloroethylidene)-β-D-tagatopyranose
CAS NO:250235-52-0
Molecular Formula:
Molecular Weight: 474.766
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)-5-O-cyclohexylcarbamoyl-1,2-O-isopropylidene-3,4-O-(2,2,2-trichloroethylidene)-β-D-tagatopyranose(CAS DataBase Reference)
NIST Chemistry Reference: (R)-5-O-cyclohexylcarbamoyl-1,2-O-isopropylidene-3,4-O-(2,2,2-trichloroethylidene)-β-D-tagatopyranose(250235-52-0)
EPA Substance Registry System: (R)-5-O-cyclohexylcarbamoyl-1,2-O-isopropylidene-3,4-O-(2,2,2-trichloroethylidene)-β-D-tagatopyranose(250235-52-0)

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: 250235-52-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 250235-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,2,3 and 5 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 250235-52:
(8*2)+(7*5)+(6*0)+(5*2)+(4*3)+(3*5)+(2*5)+(1*2)=100
100 % 10 = 0
So 250235-52-0 is a valid CAS Registry Number.

250235-52-0Upstream product

250235-52-0Downstream Products

722541-41-5 3,4-O-[(R)-ethylidene]-1,2-O-isopropylidene-5-O-(p-tosyl)-β-D-tagatopyranose

250235-52-0Relevant academic research and scientific papers

D-Tagatose derivatives from D-fructose by a facile epimerisation procedure

Frank, Michael,Miethchen, Ralf,Degenring, Daniela

, p. 167 - 170 (1999)

1,2-O-Isopropylidene-β-D-fructopyranose was directly converted into 5-O-cyclohexylcarbamoyl-1,2-O-isopropylidene-3,4-O-(2,2,2-trichloroethylidene)-β-D-tagatopyranose by treatment with chloral/N,N'-dicyclohexylcarbodiimide. Subsequent acid-catalysed cleava

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