1-HYDROXYPIPERIDINE

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CAS:4801-58-5
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Products Intro: Product Name:1-Hydroxypiperidine
CAS:4801-58-5
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Products Intro: Product Name:N-Hydroxypiperidine
CAS:4801-58-5
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CAS:4801-58-5
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1-HYDROXYPIPERIDINE manufacturers

  • 1-HYDROXYPIPERIDINE
  • 1-HYDROXYPIPERIDINE pictures
  • $9.80
  • 2020-01-09
  • CAS:4801-58-5
  • Min. Order: 1g
  • Purity: ≥99%
  • Supply Ability: 100kg
1-HYDROXYPIPERIDINE Basic information
Product Name:1-HYDROXYPIPERIDINE
Synonyms:1-HYDROXYPIPERIDINE;N-HYDROXYPIPERIDINE;1-hydroxy-piperidin;1-piperidinol;piperidin-1-ol;1-HYDROXYPIPERIDINE 96+%;1-HYDROXYPIPERDINE;1-Piperidinol/1-hydroxypiperidine
CAS:4801-58-5
MF:C5H11NO
MW:101.15
EINECS:225-362-9
Product Categories:Building Blocks;C5 to C7;Chemical Synthesis;Heterocyclic Building Blocks;Piperidines
Mol File:4801-58-5.mol
1-HYDROXYPIPERIDINE Structure
1-HYDROXYPIPERIDINE Chemical Properties
Melting point 37-39 °C
Boiling point 146-148℃ (1 Torr)
density 0.9903 (rough estimate)
refractive index 1.4550 (estimate)
Fp 78 °C
storage temp. 2-8°C
pka14.19±0.20(Predicted)
form low melting solid
color White
BRN 102726
InChI1S/C5H11NO/c7-6-4-2-1-3-5-6/h7H,1-5H2
InChIKeyLKPFBGKZCCBZDK-UHFFFAOYSA-N
SMILESON1CCCCC1
EPA Substance Registry SystemPiperidine, 1-hydroxy- (4801-58-5)
Safety Information
WGK Germany 3
RTECS TN6829550
3-10
TSCA TSCA listed
HS Code 2933399990
Storage Class11 - Combustible Solids
MSDS Information
ProviderLanguage
SigmaAldrich English
1-HYDROXYPIPERIDINE Usage And Synthesis
Chemical PropertiesSoluble in water, organic solvents, aqueous acids, and bases.
UsesBase for Fmoc-based solid phase peptide synthesis1Light stabilizing agent2
UsesBase for Fmoc-based solid phase peptide synthesis

Light stabilizing agent
Synthesis Reference(s)The Journal of Organic Chemistry, 53, p. 5856, 1988 DOI: 10.1021/jo00260a012
Synthesis
Piperidine

110-89-4

1-HYDROXYPIPERIDINE

4801-58-5

General procedure for the synthesis of N-hydroxypiperidine from hexahydropyridine: hexahydropyridine (5 mmol) and ChPS (5.5 mmol) were added to a round-bottomed flask under nitrogen protection, and the reaction was stirred for 1 hr at 60 °C. After completion of the reaction, the mixture was dissolved in water (5 mL) and the product was extracted with dichloromethane or ethyl acetate (5 mL each time, 3 times). The organic layers were combined, dried with anhydrous sodium sulfate, filtered and concentrated under reduced pressure to give the target product N-hydroxypiperidine.

References[1] Synlett, 2017, vol. 28, # 17, p. 2315 - 2319
[2] Tetrahedron Letters, 2001, vol. 42, # 20, p. 3419 - 3422
[3] Justus Liebigs Annalen der Chemie, 1948, vol. 559, p. 1,22, 23
[4] Chemische Berichte, 1951, vol. 84, p. 690,698
[5] Chemische Berichte, 1892, vol. 25, p. 2782
1-HYDROXYPIPERIDINE Preparation Products And Raw materials
Raw materials1-Ethylpiperidine-->Piperidine
Tag:1-HYDROXYPIPERIDINE(4801-58-5) Related Product Information
4-BENZOYLOXY-TEMPO 4-Hydroxy-2,2,6,6-tetramethyl-piperidinooxy 4-Amino-TEMPO, free radical 4-ACETAMIDO-TEMPO 1-HYDROXYPIPERIDINE 3,5-Dibromo-4-oxo-2,2,6,6-tetramethylpiperidin-1-yl 4-Oxo-2,2,6,6-tetramethylpiperidinooxy 2,2,6,6-Tetramethylpiperidinooxy SCOPOLAMINE N-OXIDE HYDROBROMIDE 5-(4-Hydroxypiperidino)-2-thiophenecarbaldehyde Light Stabilizer UV-622 DL-Pipecolinic acid N-BOC-4-Hydroxypiperidine (R)-4-HYDROXY-PIPERIDIN-2-ONE Ethyl 4-(4-chloro-3-(trifluoromethyl)phenyl)-4-hydroxypiperidine-1-carboxylate 4-[4-Chloro-3-(trifluoro methyl)phenyl]-4-hydroxypiperidine 4-HYDROXY-4-PHENYLPIPERIDINE 4-(4-Chlorophenyl)piperidin-4-ol