Cas 1384974-46-2,L-tert-butyl 2-[(4-(4,5-dihydro-4,4,5,5-tetramethyl-3-oxido-1H-imidazol-3-ium-1-oxyl-2-yl)phenoxy)methyl]pyrrolidine-1-carboxylate

1384974-46-2

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Product Name: L-tert-butyl 2-[(4-(4,5-dihydro-4,4,5,5-tetramethyl-3-oxido-1H-imidazol-3-ium-1-oxyl-2-yl)phenoxy)methyl]pyrrolidine-1-carboxylate
Synonyms:
CAS NO:1384974-46-2
Molecular Formula:
Molecular Weight: 432.54
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: L-tert-butyl 2-[(4-(4,5-dihydro-4,4,5,5-tetramethyl-3-oxido-1H-imidazol-3-ium-1-oxyl-2-yl)phenoxy)methyl]pyrrolidine-1-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: L-tert-butyl 2-[(4-(4,5-dihydro-4,4,5,5-tetramethyl-3-oxido-1H-imidazol-3-ium-1-oxyl-2-yl)phenoxy)methyl]pyrrolidine-1-carboxylate(1384974-46-2)
EPA Substance Registry System: L-tert-butyl 2-[(4-(4,5-dihydro-4,4,5,5-tetramethyl-3-oxido-1H-imidazol-3-ium-1-oxyl-2-yl)phenoxy)methyl]pyrrolidine-1-carboxylate(1384974-46-2)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1384974-46-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1384974-46-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,4,9,7 and 4 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1384974-46:
(9*1)+(8*3)+(7*8)+(6*4)+(5*9)+(4*7)+(3*4)+(2*4)+(1*6)=212
212 % 10 = 2
So 1384974-46-2 is a valid CAS Registry Number.

1384974-46-2Upstream product

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1384974-46-2Relevant academic research and scientific papers

Synthesis of enantiomerically pure nitronyl nitroxide radicals through chiral pool

Qin, Xiang-Yang,Ma, Yue,Wang, Qiao-Feng,Wang, Chao,Sun, Xiao-Li,Liu, Peng

, p. 314 - 319 (2012/08/28)

Two pairs of new optically active nitronyl nitroxides derived from N-Boc-D- or L- prolinol are described. The synthetic route consist of (1) the synthesis of chiral aryl aldehydes by Mitsunobu reaction, (2) the condensation of the 2,3-bis(hydroxylamino)-2

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