1-Chloro-4-iodobutane

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Names

[ CAS No. ]:
10297-05-9

[ Name ]:
1-Chloro-4-iodobutane

[Synonym ]:
Butane, 1-chloro-4-iodo-
1-Chloro-4-iodobutane
4-Iodobutyl Chloride
4-Chlorobutyl Iodide
EINECS 233-669-4
MFCD00039415

Chemical & Physical Properties

[ Density]:
1.8±0.1 g/cm3

[ Boiling Point ]:
193.6±8.0 °C at 760 mmHg

[ Melting Point ]:
93 °C

[ Molecular Formula ]:
C4H8ClI

[ Molecular Weight ]:
218.464

[ Flash Point ]:
70.9±18.4 °C

[ Exact Mass ]:
217.935913

[ LogP ]:
2.87

[ Vapour Pressure ]:
0.6±0.4 mmHg at 25°C

[ Index of Refraction ]:
1.528

MSDS

Click to get detail MSDS

Safety Information

[ Symbol ]:

GHS07

[ Signal Word ]:
Warning

[ Hazard Statements ]:
H315-H319-H335

[ Precautionary Statements ]:
P261-P305 + P351 + P338

[ Personal Protective Equipment ]:
Eyeshields;full-face respirator (US);Gloves;multi-purpose combination respirator cartridge (US);type ABEK (EN14387) respirator filter

[ Hazard Codes ]:
Xi: Irritant;

[ Risk Phrases ]:
R36/37/38

[ Safety Phrases ]:
S26-S36

[ RIDADR ]:
NONH for all modes of transport

[ WGK Germany ]:
3

Synthetic Route

Click to get detail synthetic route

Precursor & DownStream

Precursor

  • 1,4-Dichlorobutane
  • 4-Iodobutyl Tetrahydropyranyl Ether
  • 2-Octanone
  • 4-Chloro-1-butanol
  • 4-chlorobutyl methanesulfonate

DownStream

  • 1-Phenylpyrrolidine
  • Biphenyl
  • 1-chloro-4-phenylbutane
  • 5-chloro-1-phenylpentan-1-one
  • 4-Phenylbutyric acid
  • 7-chlorohept-2-yn-1-ol
  • 6-Chloro-1-hexyne
  • 1-Chloro-5-dodecyne
  • 1-Chloro-4-propoxybutane

Articles

Radical reactions with 3H-quinazolin-4-ones: synthesis of deoxyvasicinone, mackinazolinone, luotonin A, rutaecarpine and tryptanthrin.

Org. Biomol. Chem. 5(1) , 103-13, (2007)

Alkyl, aryl, heteroaryl and acyl radicals have been cyclised onto the 2-position of 3H-quinazolin-4-one. The side chains containing the radical precursors were attached to the nitrogen atom in the 3-p...

The synthesis of unsaturated fatty acids.

J. Am. Chem. Soc. 70(5) , 1699-1700., (1948)

Homogeneous catalytic reduction of a, ?-dihaloalkanes with electrogenerated nickel (I) salen. Mubarak MS and Peters DG.

J. Electroanal. Chem. 388(1) , 195-98, (1995)


More Articles

Related Compounds

  • 1-chloro-4-(cyclopenten-1-yl)benzene
  • 1-chloro-4-(1-chloro-2-methylpropan-2-yl)benzene
  • 1-chloro-4-[(1S)-1-phenylethyl]sulfanylbenzene
  • 1-chloro-4-(1,1-diethoxyethyl)benzene
  • 1-chloro-4-[(4-chlorophenyl)sulfonyl-propan-2-yloxymethyl]sulfonylbenzene
  • 1-chloro-4-[2-(4-chlorophenyl)-1,2-diphenylethenyl]benzene
  • 1-[2-methyl-3-(trifluoromethyl)phenyl]-1H-pyrrole-2-carbaldehyde
  • 3-Bromo-4-nitrophenylthiocyanate
  • 1-[3-Bromo-4-(trifluoromethoxy)phenyl]-2,2,2-trifluoroethanone
  • 5-Bromo-4-fluoro-3-(trifluoromethoxy)benzene-1,2-diamine
  • 1-[4-Bromo-3-(trifluoromethoxy)phenyl]-2,2,2-trifluoroethanone
  • 4-Fluoro-2-nitrophenylthiocyanate
  • 3-Chloro-6-[1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-yl]oxypyridazine
  • 3-Fluoro-4-nitrophenylthiocyanate
  • 2-(1-Amino-2-methoxyethyl)-5-bromophenol
  • 1-(2-Fluoro-5-iodophenyl)-2-methoxyethan-1-amine
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