Skip to Content
Merck
All Photos(1)

Key Documents

411205

Sigma-Aldrich

4-tert-Butyliodobenzene

98%

Synonym(s):

1-tert-Butyl-4-iodobenzene

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
(CH3)3CC6H4I
CAS Number:
Molecular Weight:
260.11
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.57 (lit.)

bp

116-118 °C/9 mmHg (lit.)

density

1.468 g/mL at 25 °C (lit.)

functional group

iodo

SMILES string

CC(C)(C)c1ccc(I)cc1

InChI

1S/C10H13I/c1-10(2,3)8-4-6-9(11)7-5-8/h4-7H,1-3H3

InChI key

WQVIVQDHNKQWTM-UHFFFAOYSA-N

Related Categories

General description

4-tert-Butyliodobenzene is an electron-rich aryl iodide. Heck reaction between 2-methylprop-2-en-1-ol and 4-tert-butyliodobenzene catalyzed by ionic liquids has been studied. It participates in the one-pot Heck-reductive amination reaction pathway during the synthesis of fungicide fenpropimorph.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Eye Irrit. 2

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Jungwoon Kim et al.
Molecules (Basel, Switzerland), 23(4) (2018-04-13)
Solution-processed organic light-emitting diodes (OLEDs) are attractive due to their low-cost, large area displays, and lighting features. Small molecules as well as polymers can be used as host materials within the solution-processed emitting layer. Herein, we report two 3,3'-bicarbazole-based host
One-pot multistep synthetic strategies for the production of fenpropimorph using an ionic liquid solvent.
Forsyth SA, et al.
Organic Process Research & Development, 10(1), 94-102 (2006)
Functionalised ionic liquids: synthesis of ionic liquids with tethered basic groups and their use in Heck and Knoevenagel reactions.
Forsyth SA, et al.
New. J. Chem., 34(4), 723-731 (2010)

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service