Cas 908291-77-0,ethyl 4-amino-4-N-[(1R)-phenethyl]-6,6,6-trifluoro-2,3,6-trideoxy-β-L-arabino-hexopyranoside

908291-77-0

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Basic information

Product Name: ethyl 4-amino-4-N-[(1R)-phenethyl]-6,6,6-trifluoro-2,3,6-trideoxy-β-L-arabino-hexopyranoside
Synonyms: ethyl 4-amino-4-N-[(1R)-phenethyl]-6,6,6-trifluoro-2,3,6-trideoxy-β-L-arabino-hexopyranoside
CAS NO:908291-77-0
Molecular Formula:
Molecular Weight: 333.351
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: ethyl 4-amino-4-N-[(1R)-phenethyl]-6,6,6-trifluoro-2,3,6-trideoxy-β-L-arabino-hexopyranoside(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 4-amino-4-N-[(1R)-phenethyl]-6,6,6-trifluoro-2,3,6-trideoxy-β-L-arabino-hexopyranoside(908291-77-0)
EPA Substance Registry System: ethyl 4-amino-4-N-[(1R)-phenethyl]-6,6,6-trifluoro-2,3,6-trideoxy-β-L-arabino-hexopyranoside(908291-77-0)

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: 908291-77-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 908291-77-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,2,9 and 1 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 908291-77:
(8*9)+(7*0)+(6*8)+(5*2)+(4*9)+(3*1)+(2*7)+(1*7)=190
190 % 10 = 0
So 908291-77-0 is a valid CAS Registry Number.

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908291-77-0Relevant academic research and scientific papers

A stereoselective synthesis of 6,6,6-trifluoro-l-daunosamine and 6,6,6-trifluoro-l-acosamine

Hayman, Colin M.,Larsen, David S.,Simpson, Jim,Bailey, Karl B.,Gill, Gurmit Singh

, p. 2794 - 2800 (2006)

A short synthesis of 6,6,6-trifluoro-l-acosamine 15 and 6,6,6-trifluoro-l-daunosamine 19 has been accomplished. The pyranose ring system of these carbohydrate analogues was formed by a hetero-Diels-Alder reaction of vinylogous imide 11 and ethyl vinyl eth

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