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Merck
CN

125741

Sigma-Aldrich

十氢喹啉,顺反异构体混合物

97%

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About This Item

经验公式(希尔记法):
C9H17N
CAS号:
分子量:
139.24
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:

检测方案

97%

折射率

n20/D 1.4916 (lit.)

密度

0.933 g/mL at 25 °C (lit.)

SMILES字符串

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

一般描述

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

象形图

Exclamation mark

警示用语:

Warning

预防措施声明

危险分类

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

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

154.4 °F

闪点(°C)

68 °C

个人防护装备

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

法规信息

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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
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)
The effect of phosphorus on the HDN reaction of piperidine, decahydroquinoline and ortho-propylaniline over Ni-MoS2/Al2O3 catalysts.
Jian M and Prins R.
Catalysis Letters, 35(3-4), 193-203 (1995)
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
Stephanie N Caty et al.
The Journal of experimental biology, 222(Pt 12) (2019-05-30)
Poison frogs sequester small molecule lipophilic alkaloids from their diet of leaf litter arthropods for use as chemical defenses against predation. Although the dietary acquisition of chemical defenses in poison frogs is well documented, the physiological mechanisms of alkaloid sequestration

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