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1,6-Diethyl 2,5-anhydro-3-deoxy-3-(ethoxycarbonyl)-4-C-(ethoxycarbonyl)hex-2-enarate is a complex organic compound with the molecular formula C18H24O8. It is characterized by a unique structure that includes a hex-2-enarate backbone with various functional groups. The compound features two ethoxycarbonyl groups, one attached to the 3-position and the other to the 4-C position, which contribute to its reactivity and potential applications in chemical synthesis. The anhydro and deoxy prefixes indicate the absence of water and oxygen atoms, respectively, in certain parts of the molecule. 1,6-diethyl 2,5-anhydro-3-deoxy-3-(ethoxycarbonyl)-4-C-(ethoxycarbonyl)hex-2-enarate is likely to be of interest in the field of organic chemistry, particularly for researchers studying the synthesis and properties of complex carbohydrates and their derivatives.

6307-27-3

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6307-27-3 Usage

Composition

Carbon, Hydrogen, and Oxygen atoms

Functional Groups

Ethyl and Ethoxycarbonyl groups

Functional Groups

Anhydro and Deoxy functional groups

Structural Feature

Derivative of hex-2-enarate

Potential Applications

Organic synthesis and pharmaceutical research

Further Studies

Required to determine specific properties and potential uses

Check Digit Verification of cas no

The CAS Registry Mumber 6307-27-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,0 and 7 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6307-27:
(6*6)+(5*3)+(4*0)+(3*7)+(2*2)+(1*7)=83
83 % 10 = 3
So 6307-27-3 is a valid CAS Registry Number.

6307-27-3Downstream Products

6307-27-3Relevant academic research and scientific papers

Scope and diastereoselectivity of the interrupted Feist-Benary reaction.

Calter, Michael A,Zhu, Cheng

, p. 205 - 208 (2007/10/03)

[reaction: see text] The base-promoted condensation of beta-dicarbonyl compounds with alpha-haloketones, the Feist-Benary reaction, conveniently produces highly substituted dihydrofurans. We show here that this reaction is quite general with respect to the nature of the beta-dicarbonyl compound, proceeding with beta-ketoesters, beta-oxopropionates, beta-diketones, and beta-dialdehydes. We also show that the diastereoselectivity of this reaction depends on the acidity of the nucleophile.

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