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155225

Sigma-Aldrich

2-Piperidinemethanol

97%

Sinónimos:

2-(Hydroxymethyl)piperidine

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About This Item

Fórmula empírica (notación de Hill):
C6H13NO
Número de CAS:
3433-37-2
Peso molecular:
115.17
EC Number:
222-333-2
MDL number:
MFCD00005987
UNSPSC Code:
12352100
PubChem Substance ID:
24849499
NACRES:
NA.22

assay

97%

form

solid

mp

68-70 °C (lit.)

SMILES string

OCC1CCCCN1

InChI

1S/C6H13NO/c8-5-6-3-1-2-4-7-6/h6-8H,1-5H2

InChI key

PRAYXGYYVXRDDW-UHFFFAOYSA-N

Application

2-Piperidinemethanol was used in the synthesis of 3-phenyloctahydropyrido[2,1-c][1,4]oxazine hydrochloride and the 10R and 10S diastereomers.

pictograms

Corrosion
GHS05

signalword

Danger

hcodes

H314

Hazard Classifications

Eye Dam. 1 - Skin Corr. 1B

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Sigma-Aldrich

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Sigma-Aldrich

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T N Riley et al.
Journal of medicinal chemistry, 19(2), 334-336 (1976-02-01)
3-Phenyloctahydropyrido[2,1-c][1,4]oxazine hydrochloride and the 10R and 10S diastereomers have been synthesized from (+/-)-, (+)-, and (-)-2-piperidinemethanol. Treatment of 2-piperidinemethanol with alpha-bromoacetophenone gave 3-hydroxy-3-phenyloctahydropyrido[2,1-c][1,4]oxazine which was readily converted to the 3-phenyl derivative by catalytic hydrogenolysis. These compounds were shown to possess
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