161977
N-Cyclohexylisopropylamine
98%
Synonym(s):
N-Isopropylcyclohexylamine
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About This Item
Linear Formula:
(CH3)2CHNHC6H11
CAS Number:
Molecular Weight:
141.25
Beilstein:
2070639
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
Assay
98%
form
liquid
refractive index
n20/D 1.448 (lit.)
bp
60-65 °C/12 mmHg (lit.)
density
0.859 g/mL at 25 °C (lit.)
functional group
amine
SMILES string
CC(C)NC1CCCCC1
InChI
1S/C9H19N/c1-8(2)10-9-6-4-3-5-7-9/h8-10H,3-7H2,1-2H3
InChI key
UYYCVBASZNFFRX-UHFFFAOYSA-N
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Application
N-Cyclohexylisopropylamine was used as reagent in the synthesis of 7-hydroxy cannabidiol and cannabidiol-7-oic acid.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
114.8 °F - closed cup
Flash Point(C)
46 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Raphael Mechoulam et al.
Chemistry and physics of lipids, 121(1-2), 35-43 (2002-12-31)
Over the last few years considerable attention has focused on cannabidiol (CBD), a major non-psychotropic constituent of Cannabis. In Part I of this review we present a condensed survey of the chemistry of CBD; in Part II, to be published
Ahmed A Noser et al.
Molecules (Basel, Switzerland), 25(20) (2020-10-22)
A series of novel quinazolinone derivatives (2-13) was synthesized and examined for their cytotoxicity to HepG2, MCF-7, and Caco-2 in an MTT assay. Among these derivatives, compounds 4 and 9 exhibited significant cytotoxic activity against Caco-2, HepG2, and MCF-7 cancer
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