126306
1,3-Dimethoxybenzene
≥98%
Synonym(s):
Dimethylresorcinol, Resorcinol dimethyl ether
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About This Item
Linear Formula:
C6H4(OCH3)2
CAS Number:
Molecular Weight:
138.16
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
205-783-4
Beilstein/REAXYS Number:
878582
MDL number:
Assay:
≥98%
Form:
liquid
Quality Level
assay
≥98%
form
liquid
refractive index
n20/D 1.524 (lit.)
bp
85-87 °C/7 mmHg (lit.)
density
1.055 g/mL at 25 °C (lit.)
SMILES string
COc1cccc(OC)c1
InChI
1S/C8H10O2/c1-9-7-4-3-5-8(6-7)10-2/h3-6H,1-2H3
InChI key
DPZNOMCNRMUKPS-UHFFFAOYSA-N
Application
1,3-Dimethoxybenzene has been used in the synthesis of novel oxathiane spiroketal donors. It forms pi- and O-ylidic complexes with dichlorocarbene (CCl(2)).
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Storage Class
10 - Combustible liquids
wgk
WGK 2
flash_point_f
190.4 °F - closed cup
flash_point_c
88 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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Panagiotis Stathopoulos et al.
Journal of peptide science : an official publication of the European Peptide Society, 12(3), 227-232 (2005-08-17)
Decomposition of the resin linkers during TFA cleavage of the peptides in the Fmoc strategy leads to alkylation of sensitive amino acids. The C-terminal amide alkylation, reported for the first time, is shown to be a major problem in peptide
Helena Zahradnícková et al.
Journal of separation science, 29(2), 236-241 (2006-03-10)
For the first time, headspace solid-phase microextraction coupled with GC-MS analysis was used to study volatile compounds emitted by the tick Ixodes ricinus (L.). Variables such as the type of SPME fibre, equilibration time and extraction time have been evaluated
Takashi Iijima et al.
Bioscience, biotechnology, and biochemistry, 73(11), 2547-2548 (2009-11-10)
An efficient synthesis of tri-O-methylated resveratrol is presented using an advanced Heck reaction promoted by Pd(dba)(2) in the presence of P(t-Bu)(3).
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 126306-500G | 04061838345615 |
| 126306-100G | 04061838723994 |