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2-Buten-1-one, 1-(3,4-dimethoxyphenyl)-, also known as 1-(3,4-dimethoxyphenyl)-2-buten-1-one or 3,4-dimethoxyphenyl-2-butanone, is an organic compound with the molecular formula C11H12O3. It is a colorless to pale yellow liquid with a molecular weight of 192.21 g/mol. This chemical is characterized by the presence of a 2-buten-1-one moiety (a four-carbon ketone with a double bond) and a 3,4-dimethoxyphenyl group (a phenyl ring with two methoxy groups attached at the 3rd and 4th positions). It is used as an intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other organic compounds. Due to its reactivity and functional groups, it is an important building block in organic chemistry.

4693-35-0

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4693-35-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4693-35-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,9 and 3 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 4693-35:
(6*4)+(5*6)+(4*9)+(3*3)+(2*3)+(1*5)=110
110 % 10 = 0
So 4693-35-0 is a valid CAS Registry Number.

4693-35-0Downstream Products

4693-35-0Relevant academic research and scientific papers

Synthesis of Z-alkenes from Rh(I)-catalyzed olefin isomerization of β,γ-unsaturated ketones

Zhuo, Lian-Gang,Yao, Zhong-Ke,Yu, Zhi-Xiang

, p. 4634 - 4637 (2013/10/08)

Developing olefin isomerization reactions to reach kinetically controlled Z-alkenes is challenging because formation of trans-alkenes is thermodynamically favored under the traditional catalytic conditions using acids, bases, or transition metals as the catalysts. A new synthesis of Z-alkenes from Rh(I)-catalyzed olefin isomerization of β,γ-unsaturated ketones to α,β-unsaturated ketones was developed, providing an easy and efficient way to access various Z-enones.

InBr3-Catalyzed Alkynylation and Allylation of Acid Chlorides: A Facile Synthesis of Alkynyl and Allyl Ketones

Yadav,Reddy,Reddy, M. Sridhar,Parimala

, p. 2390 - 2394 (2007/10/03)

Alkynylsilanes and allyltrimethylsilane undergo smooth coupling with acid chlorides in the presence of 5 mol% of indium tribromide under mild conditions to afford the corresponding α,β-acetylenic ketones and β,γ-unsaturated ketones in excellent yields in a short reaction time with high selectivity.

α, β-Unsaturated N-Acylureas as Useful Intermediates for the Synthesis of Indanones, Chromanones and Coumarins

Ramana, M. M. V.,Kudav, N. A.

, p. 339 - 341 (2007/10/02)

α,β-Unsaturated N-acylureas, viz-N-formamido-2-butenamide (I), N-formamido-3-methyl-2-butenamide (II) and N-formamido-3-phenyl-2-propenamide (III) react with aryl alkyl ethers in the presence of PPA to afford the corresponding crotonophenones and chalcones (IV) at lower temperature and 1-indanones (V) at a higher temperature.Reactions of I and II with phenols in the presence of PPA afford the 4-chromanones (VI), while III gives 3,4-dihydro-4-phenylcoumarins (VII) in excellent yields.

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