Cas 1187617-95-3,benzyl 7'-oxo-9'H-spiro[1,3-dioxolane-2,3'-[6]oxa[9]azabicyclo[3.3.1]nonane]-9'-carboxylate

1187617-95-3

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Basic information

Product Name: benzyl 7'-oxo-9'H-spiro[1,3-dioxolane-2,3'-[6]oxa[9]azabicyclo[3.3.1]nonane]-9'-carboxylate
Synonyms: benzyl 7'-oxo-9'H-spiro[1,3-dioxolane-2,3'-[6]oxa[9]azabicyclo[3.3.1]nonane]-9'-carboxylate
CAS NO:1187617-95-3
Molecular Formula:
Molecular Weight: 333.341
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: benzyl 7'-oxo-9'H-spiro[1,3-dioxolane-2,3'-[6]oxa[9]azabicyclo[3.3.1]nonane]-9'-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: benzyl 7'-oxo-9'H-spiro[1,3-dioxolane-2,3'-[6]oxa[9]azabicyclo[3.3.1]nonane]-9'-carboxylate(1187617-95-3)
EPA Substance Registry System: benzyl 7'-oxo-9'H-spiro[1,3-dioxolane-2,3'-[6]oxa[9]azabicyclo[3.3.1]nonane]-9'-carboxylate(1187617-95-3)

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: 1187617-95-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1187617-95-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,7,6,1 and 7 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1187617-95:
(9*1)+(8*1)+(7*8)+(6*7)+(5*6)+(4*1)+(3*7)+(2*9)+(1*5)=193
193 % 10 = 3
So 1187617-95-3 is a valid CAS Registry Number.

1187617-95-3Upstream product

1187617-94-2 benzyl 6-oxo-8H-spiro[8-azabicyclo[3.2.1]octane-3,2'-[1,3]dioxolane]-8-carboxylate

1187617-95-3Downstream Products

1187617-95-3Relevant academic research and scientific papers

Alkaloids from alkaloids: total synthesis of (±)-7a-epi-hyacinthacine A1 from Z-protected tropenone via Baeyer-Villiger oxidation

Affolter, Olena,Baro, Angelika,Frey, Wolfgang,Laschat, Sabine

scheme or table, p. 6626 - 6634 (2011/02/26)

Baeyer-Villiger oxidations of several tropane derivatives have been investigated. Whereas tropenones 15a-c underwent exclusive epoxidation to 21a-c, the corresponding 6-oxotropane derivative 28 yielded the desired lactone 29. Baeyer-Villiger oxidation was

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