What is the 2,2,6,6-Tetramethyl-4-piperidinol?

2,2,6,6-Tetramethyl-4-piperidinol is white to slightly beige crystalline powder, while it's Molecular Formula is C9H19NO. white to slightly beige crystalline powder 2,2,6,6-tetramethyl-4-piperidinol has been used to study the irradiation of Camptothecin (CPT) in aerated dimethylsulfoxide (DMSO) solution that leads to formation of singlet oxygen.

What is the CAS number for 2,2,6,6-Tetramethyl-4-piperidinol?

The CAS number of 2,2,6,6-Tetramethyl-4-piperidinol is 2403-88-5.

What is the 2,2,6,6-Tetramethyl-4-piperidinol?

2,2,6,6-Tetramethyl-4-piperidinol is white to slightly beige crystalline powder, while it's Molecular Formula is C9H19NO. white to slightly beige crystalline powder 2,2,6,6-tetramethyl-4-piperidinol has been used to study the irradiation of Camptothecin (CPT) in aerated dimethylsulfoxide (DMSO) solution that leads to formation of singlet oxygen.

What is the CAS number for 2,2,6,6-Tetramethyl-4-piperidinol?

The CAS number of 2,2,6,6-Tetramethyl-4-piperidinol is 2403-88-5.

Product classification

2403-88-5

Product Name：2,2,6,6-Tetramethyl-4-piperidinol
Molecular Formula：C₉H₁₉NO
Purity：99%
Molecular Weight：157.256

Inquiry

Product Details;

CasNo： 2403-88-5

Molecular Formula： C₉H₁₉NO

Appearance： white to slightly beige crystalline powder

Buy Quality Factory Supply 2,2,6,6-Tetramethyl-4-piperidinol 2403-88-5 with Cheap Price

Molecular Formula:C9H19NO
Molecular Weight:157.256
Appearance/Colour:white to slightly beige crystalline powder
Vapor Pressure:0.035mmHg at 25°C
Melting Point:129-131 °C(lit.)
Refractive Index:1.4248 (estimate)
Boiling Point:214.1 °C at 760 mmHg
PKA:14.99±0.60(Predicted)
Flash Point:53 °C
PSA：32.26000
Density:0.891 g/cm³
LogP:1.61670

2,2,6,6-Tetramethyl-4-piperidinol(Cas 2403-88-5) Usage

Chemical Properties	white to slightly beige crystalline powder
Uses	An intermediate in the preparation of Piperidinyloxy free radical derivatives.
Synthesis Reference(s)	The Journal of Organic Chemistry, 37, p. 2050, 1972 DOI: 10.1021/jo00977a047
Purification Methods	The piperidine crystallises from water as a hydrate and crystallises from dry ether or *C6H6 as the anhydrous base. The hydrochloride has m 282-284o (from EtOH/H2O), and the formate has m 207o(dec, from EtOH/EtOAc). [Mailey & Day J Org Chem 22 1061 1957, Beilstein 21 I 195, 21 III/IV 146, 21/1 V 159.]
Consumer Uses	ECHA has no public registered data indicating whether or in which chemical products the substance might be used. ECHA has no public registered data on the routes by which this substance is most likely to be released to the environment.

InChI:InChI=1/C9H19NO/c1-8(2)5-7(11)6-9(3,4)10-8/h7,10-11H,5-6H2,1-4H3/p+1

2403-88-5 Relevant articles

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Chen,Le Fevre

, p. 3467,3470 (1965)

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Kornblum,Pinnick

, p. 2050 (1972)

ELECTROCHEMICAL SYNTHESIS OF 2,2,6,6,-TETRAMETHYLPIPERIDINE

Kagan E. Sh.,Avrutskaya, I. A.,Kondrashov, S. V.,Novikov, V. T.,Fioshin, M. Ya.,Smirnov, V. A.

, p. 288 - 289 (1984)

A preparative method for the production ...

Reductive amination of triacetoneamine with n-butylamine over Cu-Cr-La/γ-Al2O3

Sun, Meng,Du, Xiaobao,Wang, Huabang,Wu, Zhiwei,Li, Yang,Chen, Ligong

, p. 1703 - 1708 (2011)

A series of Cu-based catalysts were prep...

Crowded piperidines with intramolecularly hydrogen-bonded nitrogen: Synthesis and conformation study

Belostotskii, Anatoly M.,Gottlieb, Hugo E.,Aped, Pinchas

, p. 3016 - 3026 (2002)

2,2,6,6-Tetramethyl substituted piperidi...

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Bellus et al.

, p. 1199 (1972)

A continuous process for the production of 2,2,6,6-tetramethylpiperidin-4- ol catalyzed by Cu-Cr/γ-Al2O3

Fan, Xiaopeng,Liu, Shuai,Yan, Xilong,Du, Xiaobao,Chen, Ligong

, p. 960 - 963 (2010)

A continuous processwas established for ...

Chemistry and anti-herpes simplex virus type 1 evaluation of 4-substituted-1H-1,2,3-triazole-nitroxyl-linked hybrids

Cunha, Anna C.,Ferreira, Vitor F.,Vaz, Maria G. F.,Cassaro, Rafael A. All?o,Resende, Jackson A. L. C.,Sacramento, Carolina Q.,Costa, Jéssica,Abrantes, Juliana L.,Souza, Thiago Moreno L.,Jord?o, Alessandro K.

, p. 2035 - 2043 (2020/05/25)

Abstract: HSV disease is distributed wor...

General methodology for the chemoselective N-alkylation of (2,2,6,6)-tetramethylpiperidin-4-ol: Contribution of microwave irradiation

Membrat, Romain,Vasseur, Alexandre,Giordano, Laurent,Martinez, Alexandre,Nuel, Didier

supporting information, p. 240 - 243 (2019/01/04)

A convenient method to access a broad va...

Phosphinous Acid Platinum Complex as Robust Catalyst for Oxidation: Comparison with Palladium and Mechanistic Investigations

Membrat, Romain,Vasseur, Alexandre,Martinez, Alexandre,Giordano, Laurent,Nuel, Didier

supporting information, p. 5427 - 5434 (2018/10/20)

Secondary phosphine oxides proved to be ...

2′-Alkynylnucleotides: A Sequence- and Spin Label-Flexible Strategy for EPR Spectroscopy in DNA

Haugland, Marius M.,El-Sagheer, Afaf H.,Porter, Rachel J.,Pe?a, Javier,Brown, Tom,Anderson, Edward A.,Lovett, Janet E.

supporting information, p. 9069 - 9072 (2016/08/05)

Electron paramagnetic resonance (EPR) sp...

2403-88-5 Process route

: 826-36-8
2,2,6,6-Tetramethyl-4-piperidone

: 109-73-9,85404-21-3
N-butylamine

: 2403-88-5
4-hydroxy-2,2,6,6-tetramethylpiperidine

: 36177-92-1
4-n-butylamino-2,2,6,6-tetramethylpiperidine

Conditions

Conditions	Yield
With hydrogen; In 1,4-dioxane; at 120 ℃; under 30003 Torr;

: 826-36-8
2,2,6,6-Tetramethyl-4-piperidone

: 36768-62-4
4-AMINO-2,2,6,6-TETRAMETHYLPIPERIDINE

: 2403-88-5
4-hydroxy-2,2,6,6-tetramethylpiperidine