The transformation of simple hydrocarbons into more complex and valuable products has revolutionised modern synthetic chemistry. This type of reactivity has quickly become one of the cornerstones of modern catalysis . 14215-68-0, Name is N-((2S,3R,4R,5R,6R)-2,4,5-Trihydroxy-6-(hydroxymethyl)tetrahydro-2H-pyran-3-yl)acetamide, molecular formula is C8H15NO6. In a Article,once mentioned of 14215-68-0, SDS of cas: 14215-68-0
Non-catalytic synthesis of 2-acetamido-2,3-dideoxy-d-erythro-hex-2- enofuranose (Chromogen I) and 3-acetamido-5-(1?,2?-dihydroxyethyl) furan (Chromogen III) from N-acetyl-d-glucosamine (GlcNAc) was achieved, with the highest yields of 23.0% and 23.1%, respectively, in high-temperature water at 120-220 C and 25 MPa with a reaction time of 7-39 s.
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Reference:
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics