4-Acetamido-2,2,6,6-tetramethyl-1-oxopiperidinium Tetrafluoroborate

Base Information

• Chemical Name: 4-Acetamido-2,2,6,6-tetramethyl-1-oxopiperidinium Tetrafluoroborate
• CAS No.: 219543-09-6
• Molecular Formula: C11H21BF4N2O2
• Molecular Weight: 0
• Hs Code.: 2933399090
• European Community (EC) Number: 677-114-8
• Wikipedia: Bobbitt%27s_salt
• Mol file: 219543-09-6.mol

Synonyms:219543-09-6;4-Acetamido-2,2,6,6-tetramethyl-1-oxopiperidinium Tetrafluoroborate;N-(2,2,6,6-tetramethyl-1-oxopiperidin-1-ium-4-yl)acetamide;tetrafluoroborate;SCHEMBL14812118;STR08344;4-acetamido-2 2 6 6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate;AKOS004908127;N-(2,2,6,6-tetramethyl-1-oxopiperidin-1-ium-4-yl)acetamide tetrafluoroborate;I11744;J-014370;4-Acetamido-2,2,6,6-tetramethyl-1-oxopiperidiniumtetrafluoroborate;4-Acetamido-2,2,6,6-tetramethyl-1-oxopiperidin-1-ium tetrafluoroborate;4-(Acetylamino)-2,2,6,6-tetramethyl-1-oxo-piperidinium tetrafluoroborate, 97%;4-acetamido-2,2,6,6-tetramethyl-1-oxo-1??-piperidin-1-ylium;tetrafluoroboranuide;N-(2,2,6,6-Tetramethyl-1-oxo-piperidin-1-ium-4-yl)acetamide tetrafluoroborate

Chemical Property of 4-Acetamido-2,2,6,6-tetramethyl-1-oxopiperidinium Tetrafluoroborate

Chemical Property:

• Melting Point: 191-197°C (decomposition)
• PSA: 70.02000
• LogP: 3.48490
• Storage Temp.: 2-8°C
• Solubility.: soluble in Methanol
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 7
• Rotatable Bond Count: 1
• Exact Mass: 300.1632207
• Heavy Atom Count: 20
• Complexity: 294

Purity/Quality:

98%,99%, ^*data from raw suppliers

N-(2,2,6,6-Tetramethyl-1-oxidopiperidin-1-ium-4-yl)acetamideTetrafluoroborate ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: [B-](F)(F)(F)F.CC(=O)NC1CC([N+](=O)C(C1)(C)C)(C)C
• Uses: Bobbitt′s salt (4-NHAc-TEMPO+ BF4 ?)?can be used as a reagent in:??????? Oxidation of alcohols to their concomitant aldehyde, ketone or carboxylic acid.?????? Conversion of aldehydes to hexafluoroisopropyl (HFIP) esters via oxidative esterification.,·???????? Deprotection of allyl ethers to corresponding aldehydes.?Preparation of α,β-unsaturated ketones by dehydrogenation of perfluoroalkyl ketones.