| Identification | More | [Name]
Ethyl iodoacetate | [CAS]
623-48-3 | [Synonyms]
ETHYL IODOACETATE
IODOACETIC ACID ETHYL ESTER
Acetic acid, iodo-, ethyl ester
ethanoicacid,iodo-,ethylester
Ethyl monoiodoacetate
ethylesterkyselinyjodoctove
ethylmonoiodoacetate
iodo-aceticaciethylester
S 9
s9
Ethyliodoacetate,98%
Ethyl iodoacetate, stabilized
2-Iodoacetic acid ethyl ester
Iodoacetic acid ethyl | [EINECS(EC#)]
210-796-3 | [Molecular Formula]
C4H7IO2 | [MDL Number]
MFCD00001081 | [Molecular Weight]
214 | [MOL File]
623-48-3.mol |
| Chemical Properties | Back Directory | [Appearance]
clear light yellow to orange liquid | [Melting point ]
<25 °C | [Boiling point ]
179-180 °C(lit.) | [density ]
1.808 g/mL at 25 °C(lit.)
| [refractive index ]
n20/D 1.503(lit.)
| [Fp ]
170 °F
| [storage temp. ]
2-8°C
| [form ]
Liquid | [color ]
Clear light yellow to orange | [Water Solubility ]
Insoluble in water. | [Sensitive ]
Light Sensitive | [BRN ]
741934 | [InChI]
1S/C4H7IO2/c1-2-7-4(6)3-5/h2-3H2,1H3 | [InChIKey]
MFFXVVHUKRKXCI-UHFFFAOYSA-N | [SMILES]
CCOC(=O)CI | [CAS DataBase Reference]
623-48-3(CAS DataBase Reference) | [EPA Substance Registry System]
Acetic acid, iodo-, ethyl ester (623-48-3) |
| Safety Data | Back Directory | [Hazard Codes ]
T | [Risk Statements ]
R25:Toxic if swallowed.
R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) . | [RIDADR ]
UN 2922 8/PG 2
| [WGK Germany ]
3
| [RTECS ]
AI3575000
| [F ]
8-19 | [TSCA ]
Yes | [HazardClass ]
6.1 | [PackingGroup ]
II | [HS Code ]
29159000 | [Storage Class]
6.1A - Combustible acute toxic Cat. 1 and 2
very toxic hazardous materials | [Hazard Classifications]
Acute Tox. 2 Oral
Eye Dam. 1
Skin Corr. 1B |
| Hazard Information | Back Directory | [Hazard]
Strong irritant to eyes and skin. | [Chemical Properties]
clear light yellow to orange liquid | [Uses]
Ethyl iodoacetate was used in the synthesis of trans-2,3-disubstituted indolines by reacting with 1-azido-2-allylbenzene derivatives via a diastereoselective radical cascade. |
|