| Identification | More | [Name]
4-Iodobenzoyl chloride | [CAS]
1711-02-0 | [Synonyms]
4-IODOBENZOYL CHLORIDE
P-IODOBENZOYL CHLORIDE
4-iodo-benzoylchlorid
Benzoyl chloride, p-iodo-
Benzoylchloride,4-iodo-
4-Iodobenzoic acid chloride | [EINECS(EC#)]
216-974-7 | [Molecular Formula]
C7H4ClIO | [MDL Number]
MFCD00001058 | [Molecular Weight]
266.46 | [MOL File]
1711-02-0.mol |
| Chemical Properties | Back Directory | [Appearance]
light yellow to beige crystalline powder and | [Melting point ]
63-65 °C (lit.) | [Boiling point ]
120-121 °C/1 mmHg (lit.) | [density ]
1.9367 (estimate) | [Fp ]
>110°C | [storage temp. ]
Keep in dark place,Inert atmosphere,Room temperature | [solubility ]
Soluble in toluene and benzene. | [form ]
Crystalline Powder and Chunks or Crystalline Mass | [color ]
Light yellow to beige | [Sensitive ]
Moisture Sensitive | [BRN ]
774718 | [InChI]
InChI=1S/C7H4ClIO/c8-7(10)5-1-3-6(9)4-2-5/h1-4H | [InChIKey]
NJAKCIUOTIPYED-UHFFFAOYSA-N | [SMILES]
C(Cl)(=O)C1=CC=C(I)C=C1 | [CAS DataBase Reference]
1711-02-0(CAS DataBase Reference) | [NIST Chemistry Reference]
Benzoyl chloride, 4-iodo-(1711-02-0) | [EPA Substance Registry System]
1711-02-0(EPA Substance) |
| Safety Data | Back Directory | [Hazard Codes ]
C | [Risk Statements ]
R34:Causes burns. | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S45:In case of accident or if you feel unwell, seek medical advice immediately (show label where possible) .
S36/37/39:Wear suitable protective clothing, gloves and eye/face protection . | [RIDADR ]
UN 3261 | [WGK Germany ]
3 | [Hazard Note ]
Corrosive/Moisture Sensitive | [TSCA ]
Yes | [HazardClass ]
8 | [PackingGroup ]
II | [HS Code ]
29163990 | [Storage Class]
8A - Combustible corrosive hazardous materials | [Hazard Classifications]
Eye Dam. 1
Skin Corr. 1B |
| Hazard Information | Back Directory | [Chemical Properties]
light yellow to beige crystalline powder and | [Uses]
4-Iodobenzoyl chloride is employed in the preparation of pyrroles by reaction with imines and acetylenes mediated by isocyanides using palladium catalysis. It is also used in the preparation of N-(1-benzylpyrrolidin-3-yl)arylbenzamides, potential human dopamine D4 antagonists. Further, it is used to prepare [2]rotaxane monomer and poly[2] rotaxane. In addition to this, it is important in the modification of poly(allylamine) in order to make the polymer X-ray visible. |
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