Cas 847555-66-2,D-1-O-cyclohexylcarbamoyl-2-deoxy-2-fluoro-3-O-methyl-5,6-O-[(R/S)-2,2,2-trichloroethylidene]-chiro-inositol

847555-66-2

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Basic information

Product Name: D-1-O-cyclohexylcarbamoyl-2-deoxy-2-fluoro-3-O-methyl-5,6-O-[(R/S)-2,2,2-trichloroethylidene]-chiro-inositol
Synonyms: D-1-O-cyclohexylcarbamoyl-2-deoxy-2-fluoro-3-O-methyl-5,6-O-[(R/S)-2,2,2-trichloroethylidene]-chiro-inositol
CAS NO:847555-66-2
Molecular Formula:
Molecular Weight: 450.719
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: D-1-O-cyclohexylcarbamoyl-2-deoxy-2-fluoro-3-O-methyl-5,6-O-[(R/S)-2,2,2-trichloroethylidene]-chiro-inositol(CAS DataBase Reference)
NIST Chemistry Reference: D-1-O-cyclohexylcarbamoyl-2-deoxy-2-fluoro-3-O-methyl-5,6-O-[(R/S)-2,2,2-trichloroethylidene]-chiro-inositol(847555-66-2)
EPA Substance Registry System: D-1-O-cyclohexylcarbamoyl-2-deoxy-2-fluoro-3-O-methyl-5,6-O-[(R/S)-2,2,2-trichloroethylidene]-chiro-inositol(847555-66-2)

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: 847555-66-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 847555-66-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,7,5,5 and 5 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 847555-66:
(8*8)+(7*4)+(6*7)+(5*5)+(4*5)+(3*5)+(2*6)+(1*6)=212
212 % 10 = 2
So 847555-66-2 is a valid CAS Registry Number.

847555-66-2Upstream product

847555-66-2Downstream Products

847673-10-3 D-1,3,4,5,6-penta-O-acetyl-2-deoxy-2-fluoro-chiro-inositol

847555-66-2Relevant academic research and scientific papers

D-2-Deoxy-2-fluoro-chiro-inositol-a new member of the deoxy fluoro inositol family

Miethchen, Ralf,Pundt, Thomas,Michalik, Manfred

, p. 831 - 833 (2005)

An efficient synthetic route to D-2-deoxy-2-fluoro-chiro-inositol has been developed with inversions of the C-1 and C-5 configuration of L-quebrachitol. The key steps of the route are two consecutive one pot epimerization procedures which do not require t

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