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Ethyl 2-ethyl-3,3-dimethyloxirane-2-carboxylate is a complex organic chemical compound with the molecular formula C9H16O3. It is a colorless liquid with a density of 0.97 g/cm3 and a boiling point of 195-200°C. ethyl 2-ethyl-3,3-dimethyloxirane-2-carboxylate is characterized by its oxirane ring, which is a three-membered cyclic ether, and a carboxylate group attached to the oxirane ring. The molecule also contains two ethyl groups and a dimethyl group, which contribute to its unique structure and properties. Ethyl 2-ethyl-3,3-dimethyloxirane-2-carboxylate is primarily used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other specialty chemicals. Its reactivity and functional groups make it a valuable building block in organic synthesis, allowing for the creation of a wide range of compounds with diverse applications.

5463-81-0

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5463-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5463-81-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,6 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 5463-81:
(6*5)+(5*4)+(4*6)+(3*3)+(2*8)+(1*1)=100
100 % 10 = 0
So 5463-81-0 is a valid CAS Registry Number.

5463-81-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name ethyl 2-ethyl-3,3-dimethyloxirane-2-carboxylate

1.2 Other means of identification

Product number -
Other names ethyl 2,3-epoxy-2-ethyl-3-methylbutanoate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:5463-81-0 SDS

5463-81-0Downstream Products

5463-81-0Relevant academic research and scientific papers

Biosynthesis of Valine and Isoleucine: Synthesis and Biological Activity of (2S)-&α-Acetolactic Acid (2-Hydroxy-2-methyl-3-oxobutanoic Acid), and (2R)- and (2S)-&α-Acetohydroxybutyric Acid (2-Ethyl-2-hydroxy-3-oxobutanoic Acid)

Armstrong, Frank B.,Lipscomb, Elizabeth L.,Crout, David H. G.,Mitchell, Michael B.,Prakash, Shimoga R.

, p. 1197 - 1202 (2007/10/02)

Stereoisomers of the two substrates for the enzyme reductoisomerase of the valine-isoleucine pathway of biosynthesis have been synthesised in optically pure form.These compounds are (2S)-α-acetolactate (2-hydroxy-2-methyl-3-oxobutanoate) and (2R)- and (2S)-α-acetohydroxybutyrate (2-ethyl-2-hydroxy-3-oxobutanoate).The synthesis of (2S)-α-acetolactate represents the first synthesis in optically pure form of the substrate of the enzyme in the valine pathway.Only the (2S)-isomers of these compounds acted as substrates for the reductoisomerase of Salmonella typhimurium.

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