Cas 906664-50-4,(-)-(1S,2aS,8bR)-8b-{2-[benzyl(tert-butoxycarbonyl)amino]ethyl}-1-[spiro-(4-γ-butyro-lactonyl)]-3-oxo-1,2,2a,3,4,8b-hexahydrocyclobuta[c]quinoline

906664-50-4

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Basic information

Product Name: (-)-(1S,2aS,8bR)-8b-{2-[benzyl(tert-butoxycarbonyl)amino]ethyl}-1-[spiro-(4-γ-butyro-lactonyl)]-3-oxo-1,2,2a,3,4,8b-hexahydrocyclobuta[c]quinoline
Synonyms:
CAS NO:906664-50-4
Molecular Formula:
Molecular Weight: 476.572
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: (-)-(1S,2aS,8bR)-8b-{2-[benzyl(tert-butoxycarbonyl)amino]ethyl}-1-[spiro-(4-γ-butyro-lactonyl)]-3-oxo-1,2,2a,3,4,8b-hexahydrocyclobuta[c]quinoline(CAS DataBase Reference)
NIST Chemistry Reference: (-)-(1S,2aS,8bR)-8b-{2-[benzyl(tert-butoxycarbonyl)amino]ethyl}-1-[spiro-(4-γ-butyro-lactonyl)]-3-oxo-1,2,2a,3,4,8b-hexahydrocyclobuta[c]quinoline(906664-50-4)
EPA Substance Registry System: (-)-(1S,2aS,8bR)-8b-{2-[benzyl(tert-butoxycarbonyl)amino]ethyl}-1-[spiro-(4-γ-butyro-lactonyl)]-3-oxo-1,2,2a,3,4,8b-hexahydrocyclobuta[c]quinoline(906664-50-4)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 906664-50-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 906664-50-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,6,6 and 4 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 906664-50:
(8*9)+(7*0)+(6*6)+(5*6)+(4*6)+(3*4)+(2*5)+(1*0)=184
184 % 10 = 4
So 906664-50-4 is a valid CAS Registry Number.

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906664-50-4Relevant academic research and scientific papers

Photochemistry of 4-(2′-aminoethyl)quinolones: Enantioselective synthesis of tetracyclic tetrahydro-1aH-pyrido[4′,3′:2,3]- cyclobuta[1,2-c] quinoline-2,11(3H,8H)-diones by intra- and intermolecular [2 + 2]-photocycloaddition reactions in solution

Selig, Philipp,Bach, Thorsten

, p. 5662 - 5673 (2006)

Enantioselective [2 + 2]-photocycloaddition reactions on 4-(2′-aminoethyl)quinolones in solution were studied using the enantiomerically pure complexing agent 1 as source of chirality. The intermolecular reactions of fully N-protected substrates 5a-5c wit

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