Cas 1394206-65-5,3-chloro-1-phenyl-2-((2,2,6,6-tetramethylpiperidin-1-yl)oxy)propan-1-one

1394206-65-5

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Basic information

Product Name: 3-chloro-1-phenyl-2-((2,2,6,6-tetramethylpiperidin-1-yl)oxy)propan-1-one
Synonyms: 3-chloro-1-phenyl-2-((2,2,6,6-tetramethylpiperidin-1-yl)oxy)propan-1-one
CAS NO:1394206-65-5
Molecular Formula:
Molecular Weight: 323.863
EINECS: N/A
Product Categories: N/A
Mol File: 1394206-65-5.mol
Article Data: 1

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: 3-chloro-1-phenyl-2-((2,2,6,6-tetramethylpiperidin-1-yl)oxy)propan-1-one(CAS DataBase Reference)
NIST Chemistry Reference: 3-chloro-1-phenyl-2-((2,2,6,6-tetramethylpiperidin-1-yl)oxy)propan-1-one(1394206-65-5)
EPA Substance Registry System: 3-chloro-1-phenyl-2-((2,2,6,6-tetramethylpiperidin-1-yl)oxy)propan-1-one(1394206-65-5)

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: 1394206-65-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1394206-65-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,9,4,2,0 and 6 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1394206-65:
(9*1)+(8*3)+(7*9)+(6*4)+(5*2)+(4*0)+(3*6)+(2*6)+(1*5)=165
165 % 10 = 5
So 1394206-65-5 is a valid CAS Registry Number.

1394206-65-5Upstream product

1394206-65-5Downstream Products

1394206-65-5Relevant articles and documents

α-aminoxylation of ketones and β-chloro-α-aminoxylation of enones with tempo and chlorocatecholborane

Li, Yi,Pouliot, Martin,Vogler, Thomas,Renaud, Philippe,Studer, Armido

supporting information, p. 4474 - 4477 (2012/10/30)

Oxidation of various cyclic and acyclic ketones under mild conditions with chlorocatecholborane, a bulky pyridine base, and TEMPO to the corresponding α-aminoxylated products in good to excellent yields (52-99%) is described. For enones as substrates, products of a β-chloro-α-aminoxylation are obtained (70-89%).

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