1,2,3-Trimethoxybenzene

Base Information Edit

Chemical Name:1,2,3-Trimethoxybenzene
CAS No.:634-36-6
Molecular Formula:C9H12O3
Molecular Weight:168.192
Hs Code.:29093090
European Community (EC) Number:211-207-2
NSC Number:10124
UNII:MRE1O894FG
DSSTox Substance ID:DTXSID1060899
Nikkaji Number:J122.021G
Wikidata:Q27159216
Metabolomics Workbench ID:67623
Mol file:634-36-6.mol

Synonyms:1,2,3-TMB;1,2,3-trimethoxybenzene

Suppliers and Price of 1,2,3-Trimethoxybenzene

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 135 raw suppliers

Chemical Property of 1,2,3-Trimethoxybenzene Edit

Chemical Property:

Appearance/Colour:white to dark beige powder
Vapor Pressure:0.0784mmHg at 25°C
Melting Point:43-47 °C(lit.)
Refractive Index:1.485
Boiling Point:235 °C at 760 mmHg
Flash Point:70.4 °C
PSA：27.69000
Density:1.041 g/cm³
LogP:1.71240
XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:168.078644241
Heavy Atom Count:12
Complexity:115

Purity/Quality:: 99% min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:
Safety Statements: S24/25:;

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Chemical Classes:Other Classes -> Ethers, Other
Canonical SMILES:COC1=C(C(=CC=C1)OC)OC
Use Description 1,2,3-Trimethoxybenzene, a chemical compound, finds applications in various fields. In the fragrance and flavor industry, it serves as an essential ingredient for the synthesis of aromatic compounds used in perfumes, colognes, and food flavorings. Its role is pivotal in enhancing the scent and taste profiles of various consumer products, providing pleasant and distinctive fragrances and flavors. Additionally, in the field of organic chemistry, this compound can be utilized as a starting material or reactant for the synthesis of complex organic molecules, contributing to academic research and the development of new chemical reactions and methodologies. Its multifaceted applications underscore its importance in improving sensory experiences in the fragrance and food industries, as well as advancing chemical research across these diverse fields.

Technology Process of 1,2,3-Trimethoxybenzene

There total 67 articles about 1,2,3-Trimethoxybenzene which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 99.0%

: 143287-98-3
3,4,5-trimethoxyphenyl trifluoromethanesulfonate

: 634-36-6
1,2,3-trimethoxybenzene

Guidance literature:: With hydrogen; diethylamine; palladium on activated charcoal; In methanol; at 20 ℃; for 4h;
DOI:10.1016/j.tet.2006.11.060

Reference yield: 99.0%

: 2675-79-8
1-bromo-3,4,5-trimethoxybenzene

: 634-36-6
1,2,3-trimethoxybenzene

Guidance literature:: With potassium hydroxide; iso-butanol; palladium diacetate; triphenylphosphine; at 100 ℃; for 1h;
DOI:10.1016/j.tet.2007.03.061

Reference yield: 95.0%

: 25245-29-8
5-iodo-1,2,3-trimethoxybenzene

: 634-36-6
1,2,3-trimethoxybenzene

Guidance literature:: With 2-(2-methoxyethoxy)ethyl alcohol; oxygen; sodium hydride; In 1,4-dioxane; at 20 ℃; for 24h; chemoselective reaction; Schlenk technique;
DOI:10.1002/anie.201601930