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5 G
$47.10
About This Item
Linear Formula:
Cl2C6H3CH2OH
CAS Number:
Molecular Weight:
177.03
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
solid
mp
79-82 °C (lit.)
functional group
chloro
hydroxyl
SMILES string
OCc1cc(Cl)cc(Cl)c1
InChI
1S/C7H6Cl2O/c8-6-1-5(4-10)2-7(9)3-6/h1-3,10H,4H2
InChI key
VSNNLLQKDRCKCB-UHFFFAOYSA-N
Application
3,5-Dichlorobenzyl alcohol was used in the preparation of 3,5-dichlorophenylacetonitrile via reaction with boiling SOCl2, followed by reaction with NaCN[1]. It was also used in the synthesis of tert-butyl 2-cyano-3-(3,5-dichlorophenyl)-propanoate via Iridium-catalysed alkylation of tert-butyl cyanoacetate[2].
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Iridium catalysed alkylation of tert-butyl cyanoacetate with alcohols under solvent free conditions.
Grigg R, et al.
Tetrahedron, 65(4), 849-854 (2009)
Esben R Sørensen et al.
Archiv der Pharmazie, 338(7), 299-304 (2005-07-05)
The HIV-1 inhibitors described in this paper is closely related to 6-(3,5-dimethylbenzyl)-1-(ethoxy methyl)-5-isopropyluracil (GCA-186) an anti-HIV-1 drug that is highly active against both wild type and mutated HIV-1 strains. The two methyl groups on the 6-benzyl moiety have been shown
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