324769-06-4

  • Product Name:1-(tert-Butoxycarbonyl)-3,3-dimethyl-4-oxopiperidine
  • Molecular Formula:C12H21NO3
  • Molecular Weight:227.304
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Product Details

Purity:99%

Manufacturer supply high quality 1-(tert-Butoxycarbonyl)-3,3-dimethyl-4-oxopiperidine 324769-06-4 with ISO standards

  • Molecular Formula:C12H21NO3
  • Molecular Weight:227.304
  • Vapor Pressure:0.001mmHg at 25°C 
  • Refractive Index:1.467 
  • Boiling Point:303.418 °C at 760 mmHg 
  • PKA:-1.51±0.40(Predicted) 
  • Flash Point:137.303 °C 
  • PSA:46.61000 
  • Density:1.035 g/cm3 
  • LogP:2.16040 

1-(TERT-BUTOXYCARBONYL)-3,3-DIMETHYL-4-OXOPIPERIDINE(Cas 324769-06-4) Usage

General Description

1-(TERT-BUTOXYCARBONYL)-3,3-DIMETHYL-4-OXOPIPERIDINE is a complex organic compound typically used in a laboratory setting due to its specific chemical properties. 1-(TERT-BUTOXYCARBONYL)-3,3-DIMETHYL-4-OXOPIPERIDINE, as its name suggests, consists of a piperidine ring, which is a saturated heterocyclic molecule. Considered a derivative of piperidine, this chemical includes additional functional groups such as a tert-butoxycarbonyl and a dimethyl group. Moreover, it also has a ketone functional group, indicated by the 4-oxo segment of the name. There is limited publicly available information regarding the specific applications or safety measures for this compound, which suggests its use is likely specialized and requires expert handling and knowledge.

InChI:InChI=1/C12H21NO3/c1-11(2,3)16-10(15)13-7-6-9(14)12(4,5)8-13/h6-8H2,1-5H3

324769-06-4 Relevant articles

Protein Modification at Tyrosine with Iminoxyl Radicals

Ishiyama, Takashi,Kanai, Motomu,Maruyama, Katsuya,Oisaki, Kounosuke,Sakai, Kentaro,Seki, Yohei,Togo, Takaya

supporting information, p. 19844 - 19855 (2021/11/30)

Post-translational modifications (PTMs) ...

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Page/Page column 20; 21, (2018/12/02)

A compound or its acid addition salt of ...

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The disclosure relates particularly to c...

324769-06-4 Process route

di-<i>tert</i>-butyl dicarbonate
24424-99-5

di-tert-butyl dicarbonate

N-benzyl-3,3-dimethylpiperidine-4-one
173186-91-9

N-benzyl-3,3-dimethylpiperidine-4-one

tert-butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylate
324769-06-4

tert-butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylate

Conditions
Conditions Yield
With hydrogen; palladium 10% on activated carbon; In methanol; at 20 ℃; for 16h; under 3345.86 Torr;
88.5%
With hydrogen; palladium/active carbon; In methanol; at 20 ℃; for 16h; under 2585.81 Torr;
88.5%
With hydrogen; palladium/active carbon; In ethanol; at 50 ℃; for 18h; under 2585.81 Torr;
56%
With hydrogen; palladium on activated charcoal; In ethanol;
palladium dihydroxide; In ethanol;
palladium dihydroxide; In ethanol;
With 10 wt% Pd(OH)2 on carbon; hydrogen; In ethanol; at 20 ℃; for 4h; under 2068.65 Torr;
methyl iodide
74-88-4

methyl iodide

tert-butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylate
324769-06-4

tert-butyl 3,3-dimethyl-4-oxopiperidine-1-carboxylate

Conditions
Conditions Yield
N-tert-butyloxycarbonylpiperidin-4-one; With sodium hydride; In tetrahydrofuran; at 0 ℃; for 0.5h;
methyl iodide; In tetrahydrofuran; at 23 ℃; for 48h;
76%

324769-06-4 Upstream products

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    N-tert-butyloxycarbonylpiperidin-4-one

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    methyl iodide

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    di-tert-butyl dicarbonate

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    N-benzyl-3,3-dimethylpiperidine-4-one

324769-06-4 Downstream products

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