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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

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.)

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

signalword

Warning

hcodes

Hazard Classifications

Flam. Liq. 3

Storage Class

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

125.6 °F - closed cup

flash_point_c

52 °C - closed cup

ppe

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


Certificates of Analysis (COA)

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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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