Cas 99655-75-1,(3R,6S,8R,9R)-9-(1-Benzenesulfonyl-1H-indol-3-ylmethyl)-3,10,10-trimethyl-2-oxa-1-aza-tricyclo[4.3.1.0<sup>3,8</sup>]decane

99655-75-1

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Basic information

Product Name: (3R,6S,8R,9R)-9-(1-Benzenesulfonyl-1H-indol-3-ylmethyl)-3,10,10-trimethyl-2-oxa-1-aza-tricyclo[4.3.1.0^3,8]decane
Synonyms:
CAS NO:99655-75-1
Molecular Formula:
Molecular Weight: 450.602
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: (3R,6S,8R,9R)-9-(1-Benzenesulfonyl-1H-indol-3-ylmethyl)-3,10,10-trimethyl-2-oxa-1-aza-tricyclo[4.3.1.0^3,8]decane(CAS DataBase Reference)
NIST Chemistry Reference: (3R,6S,8R,9R)-9-(1-Benzenesulfonyl-1H-indol-3-ylmethyl)-3,10,10-trimethyl-2-oxa-1-aza-tricyclo[4.3.1.0^3,8]decane(99655-75-1)
EPA Substance Registry System: (3R,6S,8R,9R)-9-(1-Benzenesulfonyl-1H-indol-3-ylmethyl)-3,10,10-trimethyl-2-oxa-1-aza-tricyclo[4.3.1.0^3,8]decane(99655-75-1)

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: 99655-75-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 99655-75-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,9,6,5 and 5 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 99655-75:
(7*9)+(6*9)+(5*6)+(4*5)+(3*5)+(2*7)+(1*5)=201
201 % 10 = 1
So 99655-75-1 is a valid CAS Registry Number.

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99655-75-1Relevant academic research and scientific papers

Stereocontrolled Total Syntheses of (-)-Hobartine and (+)-Aristoteline via an Intramolecular Nitrone-Olefin Cycloaddition

Gribble, Gordon W.,Barden, Timothy C.

, p. 5900 - 5902 (2007/10/02)

The Aristotelia alkaloids (-)-hobartine and (+)-aristoteline have been synthesized from indole and (S)-1-p-menthen-8-ylamine (7) in 11 steps (19percent) via an intramolecular nitrone-olefin 1,3-dipolar cycloaddition.

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