| Identification | More | [Name]
1-CHLORO-4-IODOBUTANE | [CAS]
10297-05-9 | [Synonyms]
1-CHLORO-4-IODOBUTANE
1-IODO-4-CHLOROBUTANE
TETRAMETHYLENE CHLOROIODIDE
1-chloro-4-iodo-butan
Butane, 1-chloro-4-iodo-
4-Chlorobutyl iodide | [EINECS(EC#)]
233-669-4 | [Molecular Formula]
C4H8ClI | [MDL Number]
MFCD00039415 | [Molecular Weight]
218.46 | [MOL File]
10297-05-9.mol |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [TSCA ]
Yes | [HS Code ]
29031980 |
| Hazard Information | Back Directory | [Chemical Properties]
clear yellow to brown liquid | [Uses]
1-Chloro-4-iodobutane may be used in the following studies:
- Preparation of 6-hendecenoic acid.
- Catalytic asymmetric synthesis of levobupivacaine.
- Synthesis of alkaloids such as deoxyvasicinone, mackinazolinone.
| [Uses]
1-Chloro-4-iodobutane acts as a reagent in the synthesis of alkyl chromones/quinolones via cyclization/alkylation of enaminones and as an intermediate in many pharmaceutical synthesis. | [Definition]
ChEBI: 1-Chloro-4-iodobutane is an organoiodine compound. | [General Description]
1-Chloro-4-iodobutane is a halogenated hydrocarbon. It is an α,ω-dihaloalkane and undergoes electrogenerated Nickel(I) salen (N,N′-bis(salicylidene)ethylenediamine) catalyzed reduction to afford 1,8-dichlorooctane. Electrochemical reduction of 1-chloro-4-iodobutane at glassy carbon cathode has been investigated by cyclic voltammetry and controlled-potential electrolysis. |
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