Cas 848978-60-9,(2S)-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-2-(4-chlorophenyl)-4-(trifluoromethanesulfonyloxy)-4,5-didehydro-piperidine

848978-60-9

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Basic information

Product Name: (2S)-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-2-(4-chlorophenyl)-4-(trifluoromethanesulfonyloxy)-4,5-didehydro-piperidine
Synonyms: (2S)-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-2-(4-chlorophenyl)-4-(trifluoromethanesulfonyloxy)-4,5-didehydro-piperidine
CAS NO:848978-60-9
Molecular Formula:
Molecular Weight: 840.353
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: (2S)-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-2-(4-chlorophenyl)-4-(trifluoromethanesulfonyloxy)-4,5-didehydro-piperidine(CAS DataBase Reference)
NIST Chemistry Reference: (2S)-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-2-(4-chlorophenyl)-4-(trifluoromethanesulfonyloxy)-4,5-didehydro-piperidine(848978-60-9)
EPA Substance Registry System: (2S)-N-(2,3,4,6-tetra-O-pivaloyl-β-D-galactopyranosyl)-2-(4-chlorophenyl)-4-(trifluoromethanesulfonyloxy)-4,5-didehydro-piperidine(848978-60-9)

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: 848978-60-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 848978-60-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,9,7 and 8 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 848978-60:
(8*8)+(7*4)+(6*8)+(5*9)+(4*7)+(3*8)+(2*6)+(1*0)=249
249 % 10 = 9
So 848978-60-9 is a valid CAS Registry Number.

848978-60-9Upstream product

848978-60-9Downstream Products

848978-60-9Relevant academic research and scientific papers

Palladium-catalysed C-C coupling reactions in the enantioselective synthesis of 2,4-disubstituted 4,5-dehydropiperidines using galactosylamine as a stereodifferentiating auxiliary

Knauer, Stephan,Kunz, Horst

, p. 529 - 539 (2007/10/03)

Stereoselective synthesis of enantiomerically pure 2,4-disubstituted piperidine derivatives, which are considered interesting pharmacophoric structures, was achieved starting with a tandem Mannich-Michael reaction sequence on O-pivaloylated N-galactosyl a

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