Cas 1046115-94-9,1-(1-oxyl-2,2,5,5-tetramethylpyrrolidine-3-yl)-2-hydroxymethyl-3-phenylpropane-1,3-diol

1046115-94-9

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Basic information

Product Name: 1-(1-oxyl-2,2,5,5-tetramethylpyrrolidine-3-yl)-2-hydroxymethyl-3-phenylpropane-1,3-diol
Synonyms: 1-(1-oxyl-2,2,5,5-tetramethylpyrrolidine-3-yl)-2-hydroxymethyl-3-phenylpropane-1,3-diol
CAS NO:1046115-94-9
Molecular Formula:
Molecular Weight: 322.425
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: 1-(1-oxyl-2,2,5,5-tetramethylpyrrolidine-3-yl)-2-hydroxymethyl-3-phenylpropane-1,3-diol(CAS DataBase Reference)
NIST Chemistry Reference: 1-(1-oxyl-2,2,5,5-tetramethylpyrrolidine-3-yl)-2-hydroxymethyl-3-phenylpropane-1,3-diol(1046115-94-9)
EPA Substance Registry System: 1-(1-oxyl-2,2,5,5-tetramethylpyrrolidine-3-yl)-2-hydroxymethyl-3-phenylpropane-1,3-diol(1046115-94-9)

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: 1046115-94-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1046115-94-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,6,1,1 and 5 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1046115-94:
(9*1)+(8*0)+(7*4)+(6*6)+(5*1)+(4*1)+(3*5)+(2*9)+(1*4)=119
119 % 10 = 9
So 1046115-94-9 is a valid CAS Registry Number.

1046115-94-9Upstream product

1046115-88-1 ethyl 2-{6-hydroxy-3-oxyl-2,2,4,4-tetramethyl-3-azabicyclo[3.1.0]hex-6-yl}-3-oxo-3-phenylpropanoate

1046115-94-9Downstream Products

1046115-94-9Relevant academic research and scientific papers

Synthesis of novel bicyclic nitroxides using partial favorskii rearrangement

Babi?, Andrej,Pe?ar, Slavko

, p. 1155 - 1158 (2008)

3-Bromo-2,2,6,6-tetramethyl-4-oxopiperidine-1-oxyl was reacted with several C-nucleophiles to give novel bicyclic pyrrolidine nitroxides through partial Favorskii rearrangement. Further reduction with sodium borohydride gave spin probes with free hydroxyl groups and under harsh reduction conditions allowed the Favorskii rearrangement to proceed to completion. Georg Thieme Verlag Stuttgart.

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