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Xylo-4,5-epoxy-4-methyl-6-(N-phenylcarbamoyloxy)hept-1-ene is a complex organic compound with the molecular formula C17H19NO4. It is a derivative of xylo-4,5-epoxy-4-methyl-6-hepten-1-ene, featuring a phenylcarbamoyl group attached to the hydroxyl group at the 6th carbon. This chemical is characterized by its epoxy ring, which is a three-membered ring consisting of two carbon atoms and one oxygen atom, and a methyl group at the 4th carbon. The compound's structure also includes a phenylcarbamoyl group, which is an amide derived from phenylcarboxylic acid and ammonia. This chemical is of interest in the field of organic chemistry, particularly in the synthesis of complex molecules and the study of chemical reactivity. Its potential applications may span across various industries, including pharmaceuticals, agrochemicals, and materials science, where it could be used as a building block for more complex molecules or as a precursor in the synthesis of other compounds.

97975-16-1

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97975-16-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 97975-16-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,9,7 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 97975-16:
(7*9)+(6*7)+(5*9)+(4*7)+(3*5)+(2*1)+(1*6)=201
201 % 10 = 1
So 97975-16-1 is a valid CAS Registry Number.

97975-16-1Relevant academic research and scientific papers

SYNTHESIS OF MYCAROSE AND EPI-AXENOSE FROM NON-CARBOHYDRATE PRECURSORS

Roush, William R.,Hagadorn, Susannah M.

, p. 187 - 194 (1985)

A six-step synthesis of racemic mycarose from allylacetylene is described.Key transformations include the threo-selective epoxidation of (E)-4-methyl-1,4-heptadien-6-ol and the α-opening of xylo-4,5-epoxy-4-methylhept-1-en-6-ol (7), which was accomplished

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