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N-Methyl-3-piperidinol_Molecular_structure_CAS_3554-74-3)
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N-Methyl-3-piperidinol

Catalog No. H42001 Name Sigma Aldrich
CAS Number 3554-74-3 Website http://www.sigmaaldrich.com
M. F. C6H13NO Telephone 1-800-521-8956
M. W. 115.17352 Fax
Purity 98% Email
Storage Chembase ID: 63307

SYNONYMS

Title
N-甲基-3-哌啶醇
IUPAC name
1-methylpiperidin-3-ol
IUPAC Traditional name
1-methylpiperidin-3-ol
Synonyms
1-甲基-3-哌啶醇
3-Hydroxy-1-methylpiperidine
3-羟基-1-甲基哌啶
1-Methyl-3-piperidinol

DATABASE IDS

MDL Number MFCD00006495
PubChem SID 24895628
Beilstein Number 103017
EC Number 222-609-2
CAS Number 3554-74-3

PROPERTIES

European Hazard Symbols Irritant Irritant (Xi)
MSDS Link Download
Personal Protective Equipment Eyeshields, full-face respirator (US), Gloves, multi-purpose combination respirator cartridge (US), type ABEK (EN14387) respirator filter
GHS Precautionary statements P261-P305 + P351 + P338
Risk Statements 36/37/38
Safety Statements 26-36
German water hazard class 3
GHS Pictograms GHS07
GHS Signal Word Warning
GHS Hazard statements H315-H319-H335
Empirical Formula (Hill Notation) C6H13NO
Purity 98%
Boiling Point 76-78 °C/11 mmHg(lit.)
Density 0.999 g/mL at 25 °C(lit.)
Flash Point 70 °C
Flash Point 158 °F
Refractive Index n20/D 1.474(lit.)

DETAILS

Description (English)
Packaging
25 g in glass bottle
Application
Reactant for:
• Optimization of Novobiocin scaffold to produce antitumor agents1
• Formation of carbamates and N-alkylimidazoles2Reactant for synthesis of:
• Pyridine derivatives as CDK5 inhibitors3
• Phenylcarbamate derivatives as ligands for nicotinic acetylcholine receptors4
• Amino phosphite ligands5
• Mexiletine enantiomers by nucleophilic aromatic substitution6
Description (简体中文)
包装
25 g in glass bottle
Application
Reactant for:
• Optimization of Novobiocin scaffold to produce antitumor agents1
• Formation of carbamates and N-alkylimidazoles2Reactant for synthesis of:
• Pyridine derivatives as CDK5 inhibitors3
• Phenylcarbamate derivatives as ligands for nicotinic acetylcholine receptors4
• Amino phosphite ligands5
• Mexiletine enantiomers by nucleophilic aromatic substitution6

REFERENCES