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522902

Sigma-Aldrich

(S)-(+)-2-Methylpiperidine

97%

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About This Item

Empirical Formula (Hill Notation):
C6H13N
CAS Number:
Molecular Weight:
99.17
MDL number:
UNSPSC Code:
12352005
PubChem Substance ID:
NACRES:
NA.22

assay

97%

optical activity

[α]20/D +35°, c = 3.5 in hexane

refractive index

n20/D 1.446 (lit.)

bp

117-121 °C (lit.)

density

0.823 g/mL at 25 °C (lit.)

SMILES string

C[C@H]1CCCCN1

InChI

1S/C6H13N/c1-6-4-2-3-5-7-6/h6-7H,2-5H2,1H3/t6-/m0/s1

InChI key

NNWUEBIEOFQMSS-LURJTMIESA-N

Application

(S)-(+)-2-Methylpiperidine has been used in the preparation of (S)-N-(3-(2-pipecolin-1-yl)propyl)phthalimide by reacting with N-(3-bromopropyl)phthalimide. It may also be used as a starting material in the multi-step synthesis of (2S,6S)-(+)-solenopsin A.

pictograms

FlameExclamation mark

signalword

Danger

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

60.0 °F - closed cup

flash_point_c

15.56 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


Certificates of Analysis (COA)

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Anodic Cyanation of (-)-N-Phenyl-2-Methylpiperidine: A Short Synthesis of (+)-Solenopsin A and (+)-Isosolenopsin A.
Girard N, et al.
Synthetic Communications, 35(5), 711-723 (2005)
Noncyclam Tetraamines Inhibit CXC Chemokine Receptor Type 4 and Target Glioma-Initiating Cells.
Ros-Blanco L, et al.
Journal of Medicinal Chemistry, 55(17), 7560-7570 (2012)

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