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Methyl (2E)-3-methyl-4-oxobut-2-enoate, also known as methyl 3-methyl-4-oxo-2-butenoate, is a chemical compound characterized by the molecular formula C6H8O3. It is a colorless liquid with a distinctive fruity aroma, which makes it a valuable ingredient in the flavor and fragrance industry. Its stability and non-reactivity under standard conditions contribute to its reliability in various applications, although adherence to proper handling and storage protocols is still essential for safety.

40835-18-5

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40835-18-5 Usage

Uses

Used in Flavor and Fragrance Industry:
Methyl (2E)-3-methyl-4-oxobut-2-enoate is utilized as a flavoring agent for its fruity scent, enhancing the aroma profiles of food and beverages. Its natural and pleasant odor makes it a popular choice for creating appealing taste experiences in a wide range of consumer products.
Used in Pharmaceutical Synthesis:
In the pharmaceutical sector, methyl (2E)-3-methyl-4-oxobut-2-enoate serves as a key intermediate in the synthesis of various organic compounds and drugs. Its chemical properties allow it to be a versatile building block in the development of new medications, contributing to advancements in healthcare and medicine.
Used in Chemical Research:
Methyl (2E)-3-methyl-4-oxobut-2-enoate is also employed in chemical research as a model compound for studying reactions and mechanisms. Its reactivity and stability make it suitable for exploring new chemical pathways and understanding the behavior of similar compounds in various chemical processes.

Check Digit Verification of cas no

The CAS Registry Mumber 40835-18-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,8,3 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 40835-18:
(7*4)+(6*0)+(5*8)+(4*3)+(3*5)+(2*1)+(1*8)=105
105 % 10 = 5
So 40835-18-5 is a valid CAS Registry Number.

40835-18-5Relevant articles and documents

The first synthesis of a noreremophilane isolated from the roots of Ligularia przewalskii

Reddy, D. Srinivasa,Palani, Kalpana,Balasubrahmanyam,Kamath, Viju B.,Iqbal, Javed

, p. 5211 - 5213 (2005)

The total synthesis of a natural product noreremophilane has been achieved in just three steps from readily available starting materials. A highly stereo- and regio-selective Diels-Alder reaction was the key step in our synthesis.

Simple and versatile synthesis of branched polyols: (+)-2-C-methylerythritol and (+)-2-C-methylthreitol

Fontana,Messina,Spinella,Cimino

, p. 7559 - 7562 (2007/10/03)

The paper reports a new approach for the enantioselective synthesis of 2-C-methyl tetrols. The procedure has been utilized for preparing methylthreitol and methylerythritol, a putative intermediate in the mevalonate-independent biosynthesis of terpenoids in bacteria, algae and higher plants. The methodology offers straightforward access to related compounds and isotopically labeled derivatives. (C) 2000 Elsevier Science Ltd.

Process for producing branched aldehydes

-

, (2008/06/13)

It is provided a process for industrially advantageously producing a branched aldehyde represented by the formula; STR1 ?wherein Y represents an acyl group of two or more carbon atoms; and X represents an acyloxymethyl group represented by --CH2/sub

Studies of the Synthesis of Tetronolide. Synthesis of a Spiro-α-acyltetronic Acid Model

Takeda, Kei,Shibata, Yumiko,Sagawa, Yukihiro,Urahata, Makoto,Funaki, Keishi,et al.

, p. 4673 - 4681 (2007/10/02)

The top half models 11 and 25 of the antibiotic aglycone tetronolide (1) were prepared from tetrahydrophthalide and 2,4-hexadiene-1,6-diol in 8 and 12 steps, respectively.Compound 11 was coupled with the bottom half model 30a, which was prepared via Diels-Alder reaction of methacrolein with triene 27a or 33a to afford α-acyltetronate 38.The allyl chloride 39 derived from 38 was rather unstable, and attempts for macrocyclization resulted in decomposition of the key intermediate.

A Flexible and Efficient Synthesis of Methyl 4-Oxo-2-alkenoates

Reichelt, Ingrid,Reissig, Hans-Ulrich

, p. 820 - 827 (2007/10/02)

The title compounds E are obtained in good yield by low temperature ring cleavage of the easily available methyl 2-siloxycyclopropanecarboxylates C with bromine and subsequent elimination of hydrogen bromide.Due to the variability of C a high flexibility concerning substituents R1 - R4 in products E is guaranteed. 2-Alkyl- and 2-methylthio-substituted olefins are thus effectively synthesized.In several cases the initially formed methyl 2-bromo-4-oxoalkanoates F are stable enough to be isolated in high yield.

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