478687
4-Iodophenyl isocyanate
97%
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About This Item
Fórmula lineal:
IC6H4NCO
Número de CAS:
Peso molecular:
245.02
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Productos recomendados
Quality Level
assay
97%
mp
44-48 °C (lit.)
storage temp.
2-8°C
SMILES string
Ic1ccc(cc1)N=C=O
InChI
1S/C7H4INO/c8-6-1-3-7(4-2-6)9-5-10/h1-4H
InChI key
KVMKUTIUJGYHBA-UHFFFAOYSA-N
Application
4-Iodophenyl isocyanate may be used in the preparation of:
- silicon-stereogenic silicon-bridged arylpyridinones
- N-(4-iodophenyl)cholesteryl-3-carbamate
- N-(4-iodophenyl)pregnenolone-3-carbamate
signalword
Danger
Hazard Classifications
Acute Tox. 4 Dermal - Acute Tox. 4 Inhalation - Acute Tox. 4 Oral - Eye Irrit. 2 - Resp. Sens. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
235.4 °F - closed cup
flash_point_c
113 °C - closed cup
ppe
dust mask type N95 (US), Eyeshields, Gloves
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M Van Dort et al.
International journal of radiation applications and instrumentation. Part B, Nuclear medicine and biology, 16(6), 603-607 (1989-01-01)
A series of radioiodinated benzoate and carbamate esters of cholesterol and pregnenolone wherein the acyl moiety served as the carrier for radioiodine was synthesized and evaluated as potential imaging agents for the adrenal cortex. 2,6-Dimethyl-3-iodobenzoyl and N-(4-iodophenyl) carbamoyl groups were
Rhodium-catalyzed asymmetric synthesis of silicon-stereogenic silicon-bridged arylpyridinones.
Shintani R, et al.
Chemical Science, 7, 1205-1211 (2016)
Franky Ka-Wah Hau et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 22(11), 3738-3749 (2016-02-03)
A series of mononuclear and dinuclear platinum(II) terpyridine complexes with amide-, sulfonamide-, and urea-containing ligands (1-9) has been successfully designed and synthesized, and their photophysical and anion-binding properties have been studied. The anion-binding properties of the complexes were studied by
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