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About This Item
Linear Formula:
(CH3)2C6H3CH2OH
CAS Number:
Molecular Weight:
136.19
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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![2-[(2,6-Dichlorophenyl)amino]benzaldehyde pharmaceutical impurity standard](/deepweb/assets/sigmaaldrich/product/structures/293/848/d04fb3ac-d732-41b5-99bd-b6f7fd052a25/640/d04fb3ac-d732-41b5-99bd-b6f7fd052a25.png)
assay
98%
refractive index
n20/D 1.531 (lit.)
bp
218-221 °C (lit.)
density
0.927 g/mL at 25 °C (lit.)
SMILES string
Cc1cc(C)cc(CO)c1
InChI
1S/C9H12O/c1-7-3-8(2)5-9(4-7)6-10/h3-5,10H,6H2,1-2H3
InChI key
IQWWTJDRVBWBEL-UHFFFAOYSA-N
General description
3,5-Dimethylbenzyl alcohol undergoes linear polymerization to form 1,3,5,7-tetramethyl-9,10-dihydro-anthracene[1].
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
224.6 °F - closed cup
flash_point_c
107.00 °C - closed cup
ppe
Eyeshields, Gloves
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Oligomerization of 3,5-dimethyl benzyl alcohol promoted by clay: experimental and theoretical study.
José Antonio Morales-Serna et al.
Molecules (Basel, Switzerland), 15(11), 8156-8168 (2010-11-13)
Linear oligomerization of 3,5-dimethyl benzyl alcohol is induced by a montmorillonite clay (Tonsil Optimum Extra), producing 1,3,5,7-tetramethyl-9,10-dihydro-anthracene, which, by loss of protons results in the product 1,3,5,7-tetramethylanthracene. It was also found that the compounds 4-(3´,5´-dimethylbenzyl)-1,3,5,7-tetramethyl-9,10-dihydroanthracece and 4-(3´,5´-dimethylbenzyl)-1,3,5,7-tetra-methylanthracene were formed from
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