Cas 1284207-03-9,tert-butyl (3S,3aS)-3-{[(tert-butyldiphenylsilyl)oxy]methyl}-6-methyl-5-oxo-3,3a,4,5-tetrahydro-1H-cyclopenta[c]pyrrole-2-carboxylate

1284207-03-9

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Basic information

Product Name: tert-butyl (3S,3aS)-3-{[(tert-butyldiphenylsilyl)oxy]methyl}-6-methyl-5-oxo-3,3a,4,5-tetrahydro-1H-cyclopenta[c]pyrrole-2-carboxylate
Synonyms: tert-butyl (3S,3aS)-3-{[(tert-butyldiphenylsilyl)oxy]methyl}-6-methyl-5-oxo-3,3a,4,5-tetrahydro-1H-cyclopenta[c]pyrrole-2-carboxylate
CAS NO:1284207-03-9
Molecular Formula:
Molecular Weight: 505.729
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: tert-butyl (3S,3aS)-3-{[(tert-butyldiphenylsilyl)oxy]methyl}-6-methyl-5-oxo-3,3a,4,5-tetrahydro-1H-cyclopenta[c]pyrrole-2-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: tert-butyl (3S,3aS)-3-{[(tert-butyldiphenylsilyl)oxy]methyl}-6-methyl-5-oxo-3,3a,4,5-tetrahydro-1H-cyclopenta[c]pyrrole-2-carboxylate(1284207-03-9)
EPA Substance Registry System: tert-butyl (3S,3aS)-3-{[(tert-butyldiphenylsilyl)oxy]methyl}-6-methyl-5-oxo-3,3a,4,5-tetrahydro-1H-cyclopenta[c]pyrrole-2-carboxylate(1284207-03-9)

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: 1284207-03-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1284207-03-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,8,4,2,0 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1284207-03:
(9*1)+(8*2)+(7*8)+(6*4)+(5*2)+(4*0)+(3*7)+(2*0)+(1*3)=139
139 % 10 = 9
So 1284207-03-9 is a valid CAS Registry Number.

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1284207-03-9Relevant academic research and scientific papers

Bicyclic cyclopentenones via the combination of an iridium-catalyzed allylic substitution with a diastereoselective intramolecular pauson-khand reaction

Farwick, Andreas,Engelhart, Jens U.,Tverskoy, Olena,Welter, Carolin,Umlauf Nee Stang, Quendolin A.,Rominger, Frank,Kerr, William J.,Helmchen, Guenter

, p. 349 - 370 (2011/04/18)

Enantioselective syntheses of bicyclic cyclopentenones are described. Key steps are an iridium-catalyzed allylic substitution and an intramolecular diastereoselective Pauson-Khand reaction. The diastereoselectivity of the Pauson-Khand reaction was found t

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