CAS 5673-07-4: 2,6-Dimethoxytoluene
Formula:C9H12O2
InChI:InChI=1S/C9H12O2/c1-7-8(10-2)5-4-6-9(7)11-3/h4-6H,1-3H3
InChI key:InChIKey=FPEUDBGJAVKAEE-UHFFFAOYSA-N
SMILES:O(C)C1=C(C)C(OC)=CC=C1
Synonyms:- 1,3-Dimethoxy-2-Methylbenzene
- 2-Methyl-1,3-dimethoxybenzene
- 2-Methylresorcinol dimethyl ether
- Benzene, 1,3-dimethoxy-2-methyl-
- NSC 62674
- Toluene, 2,6-dimethoxy-
- 2,6-Dimethoxytoluene
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Found 7 products.
2,6-Dimethoxytoluene
CAS:Purity:95.0%Color and Shape:Solid, CrystallineMolecular weight:152.19299316406252,6-Dimethoxytoluene
CAS:Controlled ProductApplications 2,6-Dimethoxytoluene is an organic synthesis intermediate. References Liu, C., et al.: Bioorg. Med. Chem., 24, 4263 (2016); Della S., et al.: J. Org. Chem., 81, 5726 (2016); Zhang, M., et al.: Asian J. Org. Chem., 4, 1047 (2015); Peixoto, P. A., et al.: J. Am. Chem. Soc., 136, 15248 (2014)Formula:C9H12O2Color and Shape:NeatMolecular weight:152.192,6-Dimethoxytoluene
CAS:2,6-Dimethoxytoluene is a regiospecific pentafluorophenyl compound with a thermal isomerization. It is an extractive yield that can be isolated from the reaction of acetaldehyde and formaldehyde in the presence of an imine. The process of making 2,6-dimethoxytoluene begins by reacting chloromethane with oxygenated tetrafluorobenzyne to make an intermediate. Then, this intermediate reacts with methoxylated fatty acids to create the final product. This reaction is stereoselective because it produces only one stereoisomer of 2,6-dimethoxytoluene.Formula:C9H12O2Purity:Min. 95%Color and Shape:PowderMolecular weight:152.19 g/mol1,3-Dimethoxy-2-methylbenzene
CAS:Formula:C9H12O2Purity:98%Color and Shape:SolidMolecular weight:152.190379999999982,6-Dimethoxytoluene
CAS:Formula:C9H12O2Purity:>98.0%(GC)Color and Shape:White or Colorless powder to crystalMolecular weight:152.19
