126306
1,3-Dimethoxybenzene
≥98%
Synonym(s):
Dimethylresorcinol, Resorcinol dimethyl ether
Sign In to View Organizational & Contract Pricing.
Select a Size
Change View
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)).
Still not finding the right product?
Explore all of our products under 1,3-Dimethoxybenzene
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)
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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).
Martin A Fascione et al.
Carbohydrate research, 348, 6-13 (2011-12-28)
Novel oxathiane spiroketal donors have been synthesised and activated via an umpolung S-arylation strategy using 1,3,5-trimethoxybenzene and 1,3-dimethoxybenzene. The comparative reactivity of the resulting 2,4,6-trimethoxyphenyl (TMP)- and 2,4-dimethoxyphenyl (DMP)-oxathiane spiroketal sulfonium ions is discussed, and their α-stereoselectivity in glycosylation reactions
Global Trade Item Number
| SKU | GTIN |
|---|---|
| 126306-100G | 04061838723994 |
| 126306-500G | 04061838345615 |