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But-2-enyl 1-methylallyl ether, also known as 2-butenyl 1-methylallyl ether, is a colorless liquid organic compound with the chemical formula C8H14O. It is a derivative of but-2-enol and 1-methylallyl alcohol, where the hydroxyl group of the alcohol is replaced by an ether group. but-2-enyl 1-methylallyl ether is characterized by its unique structure, which includes a conjugated diene system and an ether linkage. It is synthesized through the reaction of 1-methylallyl alcohol with but-2-enol in the presence of an acid catalyst. But-2-enyl 1-methylallyl ether is used as a chemical intermediate in the production of various organic compounds, particularly in the synthesis of fragrances and pharmaceuticals. Its properties include a boiling point of 145-146°C and a density of 0.82 g/cm3. Due to its reactivity, it is sensitive to light and heat, and should be stored in a cool, dark place.

6925-73-1

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6925-73-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6925-73-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,9,2 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6925-73:
(6*6)+(5*9)+(4*2)+(3*5)+(2*7)+(1*3)=121
121 % 10 = 1
So 6925-73-1 is a valid CAS Registry Number.

6925-73-1Downstream Products

6925-73-1Relevant academic research and scientific papers

1,2- and 1,5-Stereocontrols in 5-Hexenyl Radical Cyclizations: Cooperative or Antagonist Effect. Conformation Experimental Results with MM2 Calculations of Transition States

Bertrand, M. P.,Riggi, I. De,Lesueur, C.,Gastaldi, S.,Nouguier, R.,et al.

, p. 6040 - 6045 (1995)

The cyclofunctionalization of 1,6-dienes 1 and 2 via the addition of tosyl radical allows the analysis of the combined effects of 1,2- and 1,5-stereocontrols on the outcome of 5-hexenyl radical cyclizations.MM2 calculations of the transition states agree quite well with the experimental selectivity, i.e., exclusive 1,2-trans control, and predominance of 1,5-cis over 1,5-trans relationship.The addition of TsBr to carbohydrate-derived epimeric dienes 3a and 3b shows that the stereochemistry of the newly formed C-C bond is controlled by the configuration of the C2 center of the radical. 1,5-trans or 1,5-cis selectivity can be achieved depending on the configuration of C2.

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