162582
4,4′-Dimethoxybenzhydrol
99%
Synonym(s):
Bis(4-methoxyphenyl)carbinol
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About This Item
Linear Formula:
(CH3OC6H4)2CHOH
CAS Number:
Molecular Weight:
244.29
Beilstein/REAXYS Number:
748532
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
99%
form
powder
mp
67-70 °C (lit.)
functional group
hydroxyl
SMILES string
COc1ccc(cc1)C(O)c2ccc(OC)cc2
InChI
1S/C15H16O3/c1-17-13-7-3-11(4-8-13)15(16)12-5-9-14(18-2)10-6-12/h3-10,15-16H,1-2H3
InChI key
ZODAOVNETBTTJX-UHFFFAOYSA-N
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General description
4,4′-Dimethoxybenzhydrol causes N-alkylation of amides, lactams, carbamates, ureas and anilines in acetic acid during H2SO4 catalysis.
Application
4,4′-Dimethoxybenzhydrol was used to study the kinetics and mechanism of oxidation of substituted benzhydrols to corresponding benzophenones in the presence of Hg(OAc)2 by N-bromosuccinimide.
Storage Class
11 - Combustible Solids
wgk_germany
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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Kinetics and mechanism of oxidation of some substituted benzhydrols by N-bromosuccinimide.
Hiran BL, et al.
Kinetics and Catalysis, 46(3), 334-339 (2005)
One-Step Hydroxy Substitution of 4, 4'-Dimethoxybenzhydrol with Amides, Lactams, Carbamates, Ureas and Anilines.
Henneuse C, et al.
Synthesis, 1996(04), 495-501 (1996)
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