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Merck
CN

H42001

Sigma-Aldrich

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:
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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:
  • 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

Pictograms

Exclamation mark

Signal Word

Warning

Hazard 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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