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523496

Sigma-Aldrich

4-Iodobenzyl alcohol

97%

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About This Item

Linear Formula:
IC6H4CH2OH
CAS Number:
18282-51-4
Molecular Weight:
234.03
MDL number:
MFCD01732720
UNSPSC Code:
12352100
PubChem Substance ID:
24874338
NACRES:
NA.22

assay

97%

form

solid

mp

72-75 °C (lit.)

functional group

hydroxyl
iodo

SMILES string

OCc1ccc(I)cc1

InChI

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

InChI key

CNQRHSZYVFYOIE-UHFFFAOYSA-N

General description

4-Iodobenzyl alcohol is a benzyl alcohol derivative.

Application

4-Iodobenzyl alcohol may be used in the preparation of:
  • S-(4-Iodobenzyl) thioacetate
  • S-(4-iodobenzyl) thiobenzoate
  • fatty acid 4-iodobenzyl esters (FAIBEs)
  • (4-trimethylsilylethynylphenyl)methanol

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
MKBW5788V
MKBK1116V
MKBG1411V
MKBG1410V
MKBC3077

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Ferrocenyl Oligo (phenylene-vinylene) Thiols for the Construction of Self-Assembled Monolayers.
Amatore C, et al.
European Journal of Organic Chemistry, 25, 4035-4042 (2007)
Synthesis of a triblock copolymer containing a diacetylene group and its use for preparation of carbon nanodots.
Kim BJ, et al.
Macromolecular Research, 16(2), 103-107 (2008)
Huong T Pham et al.
Rapid communications in mass spectrometry : RCM, 27(7), 805-815 (2013-03-16)
Both traditional electron ionization and electrospray ionization tandem mass spectrometry have demonstrated limitations in the unambiguous identification of fatty acids. In the former case, high electron energies lead to extensive dissociation of the radical cations from which little specific structural
Daley R.
Organic Chemistry, 513-513 null

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