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About This Item
Linear Formula:
Cl3C6H2CH2OH
CAS Number:
Molecular Weight:
211.47
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Assay
97%
mp
98-101 °C (lit.)
SMILES string
OCc1c(Cl)cc(Cl)cc1Cl
InChI
1S/C7H5Cl3O/c8-4-1-6(9)5(3-11)7(10)2-4/h1-2,11H,3H2
InChI key
WKJWKKDGJLKFER-UHFFFAOYSA-N
Related Categories
Application
2,4,6-Trichlorobenzyl alcohol may be used in the enantioselective synthesis of sulfinite ester.2
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
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
Certificates of Analysis (COA)
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Hillary M Peltier et al.
Organic letters, 7(9), 1733-1736 (2005-04-23)
[reaction: see text] Practical reaction conditions for the catalytic enantioselective synthesis of sulfinate esters are reported. Commercially available cinchona alkaloids were found to be superior catalysts for the sulfinyl transfer reaction of tert-butanesulfinyl chloride and a variety of benzyl alcohols.
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