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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:
1556-18-9
Molecular Weight:
196.03
EC Number:
216-311-1
MDL number:
MFCD00039446
UNSPSC Code:
12352100
PubChem Substance ID:
24871251
NACRES:
NA.22

Quality Level

100

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
GHS02

Signal Word

Warning

Hazard Statements

H226

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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 4: Flammable liquids
Type 2 petroleums
Hazardous rank III
Water insoluble liquid

ISHL Indicated Name

Substances Subject to be Indicated Names

ISHL Notified Names

Substances Subject to be Notified Names

JAN Code

476412-25ML:4548173988993
476412-VAR:
476412-BULK:
476412-5ML:4548173989006

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Certificates of Analysis (COA)

Lot/Batch Number
MKCP5005
MKCL6352
MKCK7723
MKCH3988
SHBJ9333

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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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