H42001
N-Methyl-3-piperidinol
98%
Synonym(s):
1-Methyl-3-piperidinol, 3-Hydroxy-1-methylpiperidine
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About This Item
Empirical Formula (Hill Notation):
C6H13NO
CAS Number:
Molecular Weight:
115.17
Beilstein:
103017
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Assay
98%
refractive index
n20/D 1.474 (lit.)
bp
76-78 °C/11 mmHg (lit.)
density
0.999 g/mL at 25 °C (lit.)
SMILES string
CN1CCCC(O)C1
InChI
1S/C6H13NO/c1-7-4-2-3-6(8)5-7/h6,8H,2-5H2,1H3
InChI key
UKANCZCEGQDKGF-UHFFFAOYSA-N
Application
Reactant for:
Reactant for synthesis of:
- Optimization of Novobiocin scaffold to produce antitumor agents
- Formation of carbamates and N-alkylimidazoles
Reactant for synthesis of:
- Pyridine derivatives as CDK5 inhibitors
- Phenylcarbamate derivatives as ligands for nicotinic acetylcholine receptors
- Amino phosphite ligands
- Mexiletine enantiomers by nucleophilic aromatic substitution
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point(F)
158.0 °F - closed cup
Flash Point(C)
70 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Hafiz Awais Nawaz et al.
Journal of materials chemistry. B, 9(9), 2295-2307 (2021-02-23)
Injectable gelatine-based hydrogels are valuable tools for drug and cell delivery due to their extracellular matrix-like properties that can be adjusted by the degree of cross-linking. We have established anhydride-containing oligomers for the cross-linking of gelatine via anhydride-amine-conjugation. So far
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