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521590

Sigma-Aldrich

1-Chloro-5-iodopentane

97%

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About This Item

Linear Formula:
I(CH2)5Cl
CAS Number:
Molecular Weight:
232.49
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

97%

SMILES string

ClCCCCCI

InChI

1S/C5H10ClI/c6-4-2-1-3-5-7/h1-5H2

InChI key

GUUHKOCYWBEGGX-UHFFFAOYSA-N

General description

1-Chloro-5-iodopentane is a halogenated hydrocarbon. 1,10-dichlorododecane is formed as a major product from the reduction of 1-chloro-5-iodohexane with electrogenerated nickel(I) salen [salen = N,N′-bis(salicylidene)ethylenediamine]. Its IR spectra in liquid and solid states have been studied. It affords dimer radical cation on reaction with OH radicals. Synthesis of 1-chloro-5-iodopentane starting from 1,5-dichloropentane has been reported.

Application

1-Chloro-5-iodopentane may be used in the synthesis of 2-(tert-butyldimet hylsiloxy)-11-chloro-5-undecyne and cis-7-dodecen-1-ol acetate.

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Synthesis of two macrolide aggregation pheromones from the flat grain beetle, Cryptolestes pusillus (Schonherr).
Millar JC, et al.
The Journal of Organic Chemistry, 48(23), 4404-4407 (1983)
Insect sex attractants. VI. 7-dodecen-1-ol acetates and congeners.
N Green et al.
Journal of medicinal chemistry, 10(4), 533-535 (1967-07-01)
S Lindstedt et al.
Clinical chemistry, 22(8), 1330-1338 (1976-08-01)
Gas chromatography/mass spectrometry was used to identify a series of acids in urine and serum from a child who died 26 h after birth in severe metabolic acidosis with high lactate excretion. cis-5-Decene-1, 10-dioic acid and cis-5-dodencene-1, 12-dioic acid were
Conformational analysis of 1-chloro-4-iodobutane and 1-chloro-5-iodopentane.
Crowder G and Ali S.
Journal of Molecular Structure, 34(1), 47-53 (1976)
Transformation of OH-adduct of 1-chloro-4-iodobutane into intra-molecular radical cation in neutral aqueous solution.
Mohan H, et al.
Chemical Physics Letters, 300(3), 493-498 (1999)

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