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476412

Sigma-Aldrich

Iodocyclopentane

97%

Synonym(s):

Cyclopentyl iodide

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About This Item

Linear Formula:
C5H9I
CAS Number:
Molecular Weight:
196.03
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

contains

copper as stabilizer

refractive index

n20/D 1.549 (lit.)

bp

77 °C/45 mmHg (lit.)

density

1.695 g/mL at 25 °C (lit.)

functional group

iodo

SMILES string

IC1CCCC1

InChI

1S/C5H9I/c6-5-3-1-2-4-5/h5H,1-4H2

InChI key

PCEBAZIVZVIQEO-UHFFFAOYSA-N

Application

Iodocyclopentane may be used in the synthesis of 4-chloro-3′-((2-cyclopentyl-1-oxo-1,2,3,4-tetrahydroisoquinolin-6- yloxy)methyl)biphenyl-3-carboxylic acid and N-(3-methoxyphenethyl)cyclopentanamine.

Pictograms

Flame

Signal Word

Warning

Hazard Statements

Hazard Classifications

Flam. Liq. 3

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

125.6 °F - closed cup

Flash Point(C)

52 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Resonance Raman study of the A-band short-time photodissociation dynamics of axial and equatorial conformers of iodocyclopentane.
Zheng X, et al.
J. Chem. Phys. , 111(24), 11034-11043 (1999)
Raveendra-Panickar Dhanya et al.
Journal of medicinal chemistry, 54(1), 342-353 (2010-12-16)
The modification of 3'-((2-cyclopentyl-6,7-dimethyl-1-oxo-2,3-dihydro-1H-inden-5-yloxy)methyl)biphenyl-4-carboxylic acid (BINA, 1) by incorporating heteroatoms into the structure and replacing the cyclopentyl moiety led to the development of new mGluR2 positive allosteric modulators (PAMs) with optimized potency and superior druglike properties. These analogues are more

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