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558761

Sigma-Aldrich

2-Iodopyridine

98%

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About This Item

Empirical Formula (Hill Notation):
C5H4IN
CAS Number:
5029-67-4
Molecular Weight:
205.00
MDL number:
MFCD00464928
UNSPSC Code:
12352100
PubChem Substance ID:
24879772
NACRES:
NA.22
Pricing and availability is not currently available.

Quality Level

100

Assay

98%

refractive index

n20/D 1.6320 (lit.)

bp

52 °C (lit.)

density

1.928 g/mL at 25 °C (lit.)

functional group

iodo

SMILES string

Ic1ccccn1

InChI

1S/C5H4IN/c6-5-3-1-2-4-7-5/h1-4H

InChI key

CCZWSTFVHJPCEM-UHFFFAOYSA-N

Related Categories

General description

2-Iodopyridine can be synthesized from 2-chloropyridine or 2-bromopyridine via treatment with iodotrimethylsilane.[1]

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H315,H319,H335

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

Target Organs

Respiratory system

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCQ1664
MKCN4242
MKCJ7499
MKCG9578
MKBZ8227V

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Tri-(2-pyridyl) amine.
Wibaut JP and La Bastide GLC.
Rec. Trav. Chim., 52(6), 493-498 (1993)
"The solid complex Zn (CF 3) Br? 2DMF as an alternative reagent for the preparation of both, trifluoromethyl and pentafluoroethyl copper, CuCF3 and CuCF5"
Kremlev MM, et al.
Journal of Fluorine Chemistry, 131(2), 212-216 (2010)
Vibrational assignments of 2-iodopyridine.
Sortur V, et al.
Spectrochimica Acta. Part A, Molecular and Biomolecular Spectroscopy, 69(2), 604-611 (2008)
Lianzhong Luo et al.
Environmental toxicology and chemistry, 36(10), 2602-2613 (2017-03-18)
Oysters accumulate Zn as an adaptation to Zn exposure; however, it is not known whether male and female oysters respond differently to Zn exposure. Proteomic and real-time polymerase chain reaction analyses were used to investigate differential responses of male and
Photo-arylation. IV. Synthesis of 2-arylpyridines by photo-reaction of 2-iodopyridine with substituted benzenes.
Terashima M, et al.
Chemical & Pharmaceutical Bulletin, 33(3), 1009-1015 (1985)
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