Cas 271798-77-7,(1R,5R,8S)-1-(3-Benzyloxy-propyl)-8-(2,2,6,6-tetramethyl-piperidin-1-yloxy)-6-oxa-bicyclo[3.2.1]octane-2,7-dione

271798-77-7

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Basic information

Product Name: (1R,5R,8S)-1-(3-Benzyloxy-propyl)-8-(2,2,6,6-tetramethyl-piperidin-1-yloxy)-6-oxa-bicyclo[3.2.1]octane-2,7-dione
Synonyms: (1R,5R,8S)-1-(3-Benzyloxy-propyl)-8-(2,2,6,6-tetramethyl-piperidin-1-yloxy)-6-oxa-bicyclo[3.2.1]octane-2,7-dione
CAS NO:271798-77-7
Molecular Formula:
Molecular Weight: 443.583
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: (1R,5R,8S)-1-(3-Benzyloxy-propyl)-8-(2,2,6,6-tetramethyl-piperidin-1-yloxy)-6-oxa-bicyclo[3.2.1]octane-2,7-dione(CAS DataBase Reference)
NIST Chemistry Reference: (1R,5R,8S)-1-(3-Benzyloxy-propyl)-8-(2,2,6,6-tetramethyl-piperidin-1-yloxy)-6-oxa-bicyclo[3.2.1]octane-2,7-dione(271798-77-7)
EPA Substance Registry System: (1R,5R,8S)-1-(3-Benzyloxy-propyl)-8-(2,2,6,6-tetramethyl-piperidin-1-yloxy)-6-oxa-bicyclo[3.2.1]octane-2,7-dione(271798-77-7)

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: 271798-77-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 271798-77-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,7,1,7,9 and 8 respectively; the second part has 2 digits, 7 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 271798-77:
(8*2)+(7*7)+(6*1)+(5*7)+(4*9)+(3*8)+(2*7)+(1*7)=187
187 % 10 = 7
So 271798-77-7 is a valid CAS Registry Number.

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271798-77-7Relevant academic research and scientific papers

TEMPO free radical derived β-aminoalkoxyketolactones: Substrates for base-, acid- and radical-induced fragmentation reactions

Schultz, Arthur G.,Zhang, Xuqing

, p. 399 - 400 (2000)

β-Aminoalkoxyketolactones 2 and 3 obtained from the TEMPO free radical substitution of iodolactones 1 undergo fragmentations under basic, acidic and free radical conditions.

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