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529982

Sigma-Aldrich

2-Iodobiphenyl

96%

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About This Item

Linear Formula:
C6H5C6H4l
CAS Number:
2113-51-1
Molecular Weight:
280.10
EC Number:
218-303-3
MDL number:
MFCD00039396
UNSPSC Code:
12352100
PubChem Substance ID:
24877721
NACRES:
NA.22

Assay

96%

refractive index

n20/D 1.662 (lit.)

bp

300 °C (lit.)

density

1.59 g/mL at 25 °C (lit.)

functional group

iodo
phenyl

SMILES string

Ic1ccccc1-c2ccccc2

InChI

1S/C12H9I/c13-12-9-5-4-8-11(12)10-6-2-1-3-7-10/h1-9H

InChI key

QFUYDAGNUJWBSM-UHFFFAOYSA-N

General description

2-Iodobiphenyl is an ortho-halogenated biphenyl that can be synthesized from 2-aminobiphenyl.

Application

2-Iodobiphenyl may be used in the synthesis of dibenziodolium tosylate by reacting with hydroxy(tosyloxy)iodo] benzene in acetonitrile.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV4908
MKBC1575V
MKBV4302V
MKBS3820V
MKBM1410V

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Dicyclic Hydrocarbons. I. 2-Aklylbiphenyls.
Goodman IA and Wise PH.
Journal of the American Chemical Society, 72(7), 3076-3079 (1950)
[Hydroxy (tosyloxy) iodo] benzene, a versatile reagent for the mild oxidation of aryl iodides at the iodine atom by ligand transfer.
Koser GF and Wettach RH.
The Journal of Organic Chemistry, 45(8), 1542-1543 (1980)
Michael Barclay et al.
Physical chemistry chemical physics : PCCP, 21(8), 4556-4567 (2019-02-12)
We present a combined theoretical and experimental study on the ionization and primary fragmentation channels of the mono-halogenated biphenyls; 2-chlorobiphenyl, 2-bromobiphenyl and 2-iodobiphenyl. The ionization energies (IEs) of the 2-halobiphenyls and the appearance energies (AEs) of the principal fragments are

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