All Photos(1)
Synonym(s):
2-Hydroxyethyl iodide, 2-Iodoethan-1-ol, Ethylene iodohydrin
Linear Formula:
ICH2CH2OH
CAS Number:
Molecular Weight:
171.97
Beilstein:
1098258
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
99%
form
liquid
contains
copper as stabilizer
refractive index
n20/D 1.572 (lit.)
bp
85 °C/25 mmHg (lit.)
density
2.205 g/mL at 25 °C (lit.)
storage temp.
2-8°C
SMILES string
OCCI
InChI
1S/C2H5IO/c3-1-2-4/h4H,1-2H2
InChI key
QSECPQCFCWVBKM-UHFFFAOYSA-N
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General description
The standard molar enthalpy of 2-iodoethanol formation has been studied.
Application
2-Iodoethanol was used in the synthesis of the neuroexcitants 3-(carboxymethyl)pyrrolidine-2,4-dicarboxylic acid, α-kainic acid, alpha-isokainic acid and alpha-dihydroallokainic acid.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 2 Oral
WGK
WGK 3
Flash Point(F)
closed cup
Flash Point(C)
closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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David M Hodgson et al.
The Journal of organic chemistry, 70(22), 8866-8876 (2005-10-22)
[reaction; see text] N-Boc syn-7-(2-hydroxyethyl)-4-(alkyl or aryl)sulfonyl-2-azabicyclo[2.2.1]hept-5-enes serve as precursors in syntheses of the neuroexcitants 3-(carboxymethyl)pyrrolidine-2,4-dicarboxylic acid 43, alpha-kainic acid 12, alpha-isokainic acid 14, and alpha-dihydroallokainic acid 77. The key step in these syntheses is the intermolecular radical addition of
Carlos E S Bernardes et al.
The journal of physical chemistry. A, 111(9), 1713-1720 (2007-02-10)
The energetics of the C-F, C-Cl, C-Br, and C-I bonds in 2-haloethanols was investigated by using a combination of experimental and theoretical methods. The standard molar enthalpies of formation of 2-chloro-, 2-bromo-, and 2-iodoethanol, at 298.15 K, were determined as
Abdullah M Alswieleh et al.
Designed monomers and polymers, 22(1), 226-235 (2019-12-20)
Poly(2‑(tert-butylamino)ethyl methacrylate) brushes (PTBAEMA) are grown from mesoporous silica nanoparticles via surface-initiated atom transfer radical polymerization (SI-ATRP). Linear PTBAEMA brushes are protonated and highly swollen at low pH; brushes are collapsed at pH higher than 7.7 due to deprotonation, as
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