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529982

Sigma-Aldrich

2-Iodobiphenyl

96%

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25 G
¥31,100

¥31,100

Estimated to ship onApril 11, 2025Details

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25 G
¥31,100

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

¥31,100

Estimated to ship onApril 11, 2025Details

Request a Bulk Order

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

Related Categories

General description

2-Iodobiphenyl is an ortho-halogenated biphenyl that can be synthesized from 2-aminobiphenyl.[1]

Application

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

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

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 3 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

529982-BULK:
529982-VAR:
529982-25G:4548173994628

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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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