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161977

Sigma-Aldrich

N-Cyclohexylisopropylamine

98%

Synonym(s):

N-Isopropylcyclohexylamine

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About This Item

Linear Formula:
(CH3)2CHNHC6H11
CAS Number:
1195-42-2
Molecular Weight:
141.25
Beilstein:
2070639
EC Number:
214-798-5
MDL number:
MFCD00003831
UNSPSC Code:
12352100
PubChem Substance ID:
24849964

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.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319,H335

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

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Certificates of Analysis (COA)

Lot/Batch Number
MKBZ1867V
MKBW5858V
MKBV2169V
MKBV0926V
MKBT8880V

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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
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

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