I agree Our site saves small pieces of text information (cookies) on your device in order to deliver better content and for statistical purposes. You can disable the usage of cookies by changing the settings of your browser. By browsing our website without changing the browser settings you grant us permission to store that information on your device.
Glucose was transformed to various furan compounds and carboxylic acids derivatives by heat treatment of autoclave such as levulinic acid, 2-acetylfuran and 2-acetyl-5-methylfuran. using 2-acetyl-5-methylfuran or 1,5-dimethyl-2-pyrrolecarbonitrile as reactants, that the formation of the 4-arylation products. Reaction of 2-acetyl-5-methylfuran 6a with 2-aminoethanol pioduced in 79% yield the aminal.
Keith Basey,; Jack G. Woolley. Alkaloids of Physalis alkekengi. Phytochemistry. 1973, 12 (10), 2557-2559.
Liang Zhang,; Isao Kuniyoshi,; Mitsuyo Hirai,; Makoto Shoda. Oxidation of dimethyl sulfide byPseudomonas acidovorans DMR-11 isolated from peat biofilter. Biotechnology Letters. 1991, 13 (3), 223-228.
Hazard Statements: H227-H302
Combustible liquid. Harmful if swallowed.
Precautionary Statements: P210-P264b-P270-P280-P301+P312-P330-P370+P378q-P501c
Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Wash face, hands and any exposed skin thoroughly after handling Do not eat, drink or smoke when using this product. Wear protective gloves/protective clothing/eye protection/face protection. IF SWALLOWED: Call a POISON CENTER or doctor/physician if you feel unwell. Rinse mouth. In case of fire: Use CO2, dry chemical, or foam Dispose of contents/ container to an approved waste disposal plant