Cas 1097643-41-8,(S)-2-phenyl-4-oxa-1-aza-13-azonia-bicyclo[11.2.1]hexadeca-13<sup>(16)</sup>,14-diene chloride

1097643-41-8

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Basic information

Product Name: (S)-2-phenyl-4-oxa-1-aza-13-azonia-bicyclo[11.2.1]hexadeca-13⁽¹⁶⁾,14-diene chloride
Synonyms:
CAS NO:1097643-41-8
Molecular Formula:
Molecular Weight: 334.889
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: (S)-2-phenyl-4-oxa-1-aza-13-azonia-bicyclo[11.2.1]hexadeca-13⁽¹⁶⁾,14-diene chloride(CAS DataBase Reference)
NIST Chemistry Reference: (S)-2-phenyl-4-oxa-1-aza-13-azonia-bicyclo[11.2.1]hexadeca-13⁽¹⁶⁾,14-diene chloride(1097643-41-8)
EPA Substance Registry System: (S)-2-phenyl-4-oxa-1-aza-13-azonia-bicyclo[11.2.1]hexadeca-13⁽¹⁶⁾,14-diene chloride(1097643-41-8)

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: 1097643-41-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1097643-41-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,9,7,6,4 and 3 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1097643-41:
(9*1)+(8*0)+(7*9)+(6*7)+(5*6)+(4*4)+(3*3)+(2*4)+(1*1)=178
178 % 10 = 8
So 1097643-41-8 is a valid CAS Registry Number.

1097643-41-8Upstream product

1097643-39-4 (S)-1-[2-(8-chlorooctyloxy)-1-phenylethyl]imidazole

1097643-41-8Downstream Products

1097643-41-8Relevant academic research and scientific papers

Cyclophane-type imidazolium salts with planar chirality as a new class of N-heterocyclic carbene precursors

Matsuoka, Yuki,Ishida, Yasuhiro,Sasaki, Daisuke,Saigo, Kazuhiko

supporting information; experimental part, p. 9215 - 9222 (2009/10/01)

Cyclophane-type imidazolium salts with planar chirality were synthesized from enantiopure 2-amino alcohols, of which the N(1) and N(3) positions were connected with a bridge. The structural profiles of the imidazolium salts and their derivative N-heterocy

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