Skip to Content
Merck
All Photos(2)

Key Documents

View All Documentation

183636

Sigma-Aldrich

2-Iodobenzyl alcohol

98%

Sign Into View Organizational & Contract Pricing
All Photos(2)

About This Item

Linear Formula:
IC6H4CH2OH
CAS Number:
5159-41-1
Molecular Weight:
234.03
Beilstein:
2079487
EC Number:
225-933-2
MDL number:
MFCD00004610
UNSPSC Code:
12352100
PubChem Substance ID:
24851064
NACRES:
NA.22

Quality Level

100

Assay

98%

mp

89-92 °C (lit.)

functional group

hydroxyl
iodo

SMILES string

OCc1ccccc1I

InChI

1S/C7H7IO/c8-7-4-2-1-3-6(7)5-9/h1-4,9H,5H2

InChI key

WZCXOBMFBKSSFA-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

2-Iodobenzyl alcohol was used in the synthesis of:
  • substituted seven-membered lactones
  • 2-[(E)-(1′-iodo-2′-propenyl)]benzyl alcohol
  • 2,3-diphenyl-1-indenone

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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
MKCW4687
MKBQ9969V
MKCL4476
MKCC4701
16925LH

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.

Search for a COA

Already Own This Product?

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

Visit the Document Library

Guangwei Wang et al.
Journal of organometallic chemistry, 692(21), 4731-4736 (2007-10-01)
The Zr-catalyzed methylalumination of heterosubstituted arylethynes containing O, S, Cl, and Si can proceed in high yields (>70%) and in a highly regio- and stereoselective manner (≥98-99%), although SO(2)Ph, Br, and Cl in a benzylic position present serious chemoselectivity-related problems.
Dinesh Kumar Rayabarapu et al.
Journal of the American Chemical Society, 124(20), 5630-5631 (2002-05-16)
A new class of substituted seven-membered lactones 3 were conveniently synthesized via cyclization of o-iodobenzyl alcohol 1 (o-IC(6)H(4)CH(2)OH) with various propiolates 2 (RC triple bond CCOOMe) in the presence of Ni(dppe)Br(2) and Zn powder in acetonitrile at 80 degrees C.
Synthesis of indenones via palladium-catalyzed annulation of internal alkynes.
Larock RC, et al.
The Journal of Organic Chemistry, 58(17), 4579-4583 (1993)

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