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Merck
CN

125741

Decahydroquinoline, mixture of cis and trans

97%

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About This Item

Empirical Formula (Hill Notation):
C9H17N
CAS Number:
Molecular Weight:
139.24
UNSPSC Code:
12352100
PubChem Substance ID:
EC Number:
218-116-7
MDL number:
Assay:
97%
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assay

97%

refractive index

n20/D 1.4916 (lit.)

density

0.933 g/mL at 25 °C (lit.)

SMILES string

C1CCC2NCCCC2C1

InChI

1S/C9H17N/c1-2-6-9-8(4-1)5-3-7-10-9/h8-10H,1-7H2

InChI key

POTIYWUALSJREP-UHFFFAOYSA-N

General description

Hydrodenitrogenation of decahydroquinoline has been investigated over Ni-MoS2/γ-Al2O3 and NiMo(P)/Al2O3 catalysts.


pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

154.4 °F - closed cup

flash_point_c

68 °C - closed cup

ppe

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

Regulatory Information

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Ring opening of 1, 2, 3, 4-tetrahydroquinoline and decahydroquinoline on MoS2/γ-Al2O3 and Ni-MoS2/γ-Al2O3.
Gutierrez OY, et al.
J. Catal., 295, 155-168 (2012)
Lauren A O'Connell et al.
The Journal of experimental biology, 224(Pt 3) (2021-01-08)
Poison frogs sequester chemical defenses from their diet of leaf litter arthropods for defense against predation. Little is known about the physiological adaptations that confer this unusual bioaccumulation ability. We conducted an alkaloid-feeding experiment with the Diablito poison frog (Oophaga
Savithra Jayaraj et al.
Scientific reports, 9(1), 11280-11280 (2019-08-04)
Visible-light mediated aerobic dehydrogenation of N-heterocyclic compounds is a reaction with enormous potential for application. Herein, we report the first complete aerobic dehydrogenation pathway to large-scale production of isoquinolines. The discovery of this visible light photoredox reaction was enabled through