Cas 1201926-49-9,(1S,2S,5R,7S)-1-allyl-2,5-dimethyl-3-tosyl-7-(2,4,6-trimethoxyphenyl)-9-oxa-3-azabicyclo[3.3.1]nonane

1201926-49-9

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Basic information

Product Name: (1S,2S,5R,7S)-1-allyl-2,5-dimethyl-3-tosyl-7-(2,4,6-trimethoxyphenyl)-9-oxa-3-azabicyclo[3.3.1]nonane
Synonyms: (1S,2S,5R,7S)-1-allyl-2,5-dimethyl-3-tosyl-7-(2,4,6-trimethoxyphenyl)-9-oxa-3-azabicyclo[3.3.1]nonane
CAS NO:1201926-49-9
Molecular Formula:
Molecular Weight: 515.671
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,2S,5R,7S)-1-allyl-2,5-dimethyl-3-tosyl-7-(2,4,6-trimethoxyphenyl)-9-oxa-3-azabicyclo[3.3.1]nonane(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2S,5R,7S)-1-allyl-2,5-dimethyl-3-tosyl-7-(2,4,6-trimethoxyphenyl)-9-oxa-3-azabicyclo[3.3.1]nonane(1201926-49-9)
EPA Substance Registry System: (1S,2S,5R,7S)-1-allyl-2,5-dimethyl-3-tosyl-7-(2,4,6-trimethoxyphenyl)-9-oxa-3-azabicyclo[3.3.1]nonane(1201926-49-9)

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: 1201926-49-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1201926-49-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,1,9,2 and 6 respectively; the second part has 2 digits, 4 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1201926-49:
(9*1)+(8*2)+(7*0)+(6*1)+(5*9)+(4*2)+(3*6)+(2*4)+(1*9)=119
119 % 10 = 9
So 1201926-49-9 is a valid CAS Registry Number.

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1201926-49-9Relevant academic research and scientific papers

Gold- or platinum-catalyzed cascade processes of alkynol derivatives involving hydroalkoxylation reactions followed by prins-type cyclizations

Barluenga, Jose,Fernandez, Amadeo,Dieguez, Alejandro,Rodriguez, Felix,Fananas, Francisco J.

supporting information; experimental part, p. 11660 - 11667 (2010/04/28)

An efficient method for the synthesis of [3.3.1]bicyclic compounds from easily available alkynol derivatives has been developed. The reaction is based on a gold- or platinum-catalyzed tandem process that involves an intramolecular hydroalkoxylation of a t

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