262595
Perhydroisoquinoline
96%
Synonym(s):
Decahydroisoquinoline
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About This Item
Empirical Formula (Hill Notation):
C9H17N
CAS Number:
Molecular Weight:
139.24
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
assay
96%
composition
(mixture of cis and trans)
refractive index
n20/D 1.4904 (lit.)
bp
211-214 °C (lit.)
density
0.936 g/mL at 25 °C (lit.)
SMILES string
C1CCC2CNCCC2C1
InChI
1S/C9H17N/c1-2-4-9-7-10-6-5-8(9)3-1/h8-10H,1-7H2
InChI key
NENLYAQPNATJSU-UHFFFAOYSA-N
General description
Spectroscopic investigations of charge-transfer complexes of perhydroisoquinoline with 2,3-dichloro-5,6-dicyano-1,4-benzoquinone, p-chloranil and 7,7′,8,8′-tetracyanoquinodimethane has been reported.
Application
Perhydroisoquinoline has been used in the synthesis of nelfinavir mesylate.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
174.2 °F - closed cup
flash_point_c
79 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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Spectroscopic and thermal studies on charge-transfer complexes of perhydroisoquinoline with p-chloranil, 2, 3-dichloro-5, 6-dicyano-1, 4-benzoquinone, and 7, 7', 8, 8'-tetracyanoquinodimethane.
Refat MS and Abou-Melha S.
Journal of Applied Spectroscopy, 79(1), 11-21 (2012)
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
Thomas Körber et al.
Physical chemistry chemical physics : PCCP, 22(16), 9086-9097 (2020-04-18)
A series of high-Tg glass formers with Tg values varying between 347 and 390 K and molar masses in the range of 341 and 504 g mol-1 are investigated by dielectric spectroscopy. They are compared to paradigmatic reference systems. Differently
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Noncontact ratiometric fluorescent thermometers have received great interests in recent years. Besides being a sensitive and easily observable detection signal, the ratiometric dual fluorescence are also highly accurate and resistable to interference. However, organic molecular thermometers with such fluorescence property
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Journal of medicinal chemistry, 63(23), 14780-14804 (2020-11-20)
The tyrosine phosphatase SHP2 controls the activity of pivotal signaling pathways, including MAPK, JAK-STAT, and PI3K-Akt. Aberrant SHP2 activity leads to uncontrolled cell proliferation, tumorigenesis, and metastasis. SHP2 signaling was recently linked to drug resistance against cancer medications such as
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