155225
2-Piperidinemethanol
97%
Synonym(s):
2-(Hydroxymethyl)piperidine
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About This Item
Empirical Formula (Hill Notation):
C6H13NO
CAS Number:
Molecular Weight:
115.17
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
222-333-2
MDL number:
Product Name
2-Piperidinemethanol, 97%
InChI key
PRAYXGYYVXRDDW-UHFFFAOYSA-N
InChI
1S/C6H13NO/c8-5-6-3-1-2-4-7-6/h6-8H,1-5H2
SMILES string
OCC1CCCCN1
assay
97%
form
solid
mp
68-70 °C (lit.)
functional group
hydroxyl
Quality Level
Related Categories
Application
2-Piperidinemethanol was used in the synthesis of 3-phenyloctahydropyrido[2,1-c][1,4]oxazine hydrochloride and the 10R and 10S diastereomers.
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Mostafa Hadei et al.
Journal of occupational medicine and toxicology (London, England), 13, 30-30 (2018-10-03)
The use of cosmetic products in beauty salons emits numerous kinds of toxic air pollutants. The objectives of this study were to measure the concentrations of benzene, toluene, ethylbenzene, xylene, formaldehyde, and acetaldehyde in 20 large beauty salons in Tehran
Daniel C O'Brien et al.
Otolaryngology--head and neck surgery : official journal of American Academy of Otolaryngology-Head and Neck Surgery, 163(3), 508-516 (2020-05-27)
To assess the exposure of surgical personnel to known carcinogens during pediatric tonsillectomy and adenoidectomy (T&A) and compare the efficacy of surgical smoke evacuation systems during T&A. Prospective, case series. Tertiary children's hospital. The present study assessed operating room workers'
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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