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2-((E)-3-Oxo-propenyl)-benzoic acid methyl ester is a chemical compound with the molecular formula C11H10O4. It is an organic ester derived from benzoic acid, featuring a methyl ester group and a conjugated enone side chain. 2-((E)-3-Oxo-propenyl)-benzoic acid methyl ester is characterized by its aromatic ring structure, with a carbonyl group at the 2-position and an (E)-3-oxo-propenyl group attached to it. The (E)-configuration indicates that the double bond in the propenyl group has a trans arrangement. This chemical is known for its potential applications in the synthesis of various pharmaceuticals and other organic compounds, due to its reactive functional groups and structural diversity.

78024-61-0

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78024-61-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 78024-61-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,0,2 and 4 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 78024-61:
(7*7)+(6*8)+(5*0)+(4*2)+(3*4)+(2*6)+(1*1)=130
130 % 10 = 0
So 78024-61-0 is a valid CAS Registry Number.

78024-61-0Relevant academic research and scientific papers

Organocatalytic Kinetic Resolution of Sulfoximines

Dong, Shunxi,Frings, Marcus,Cheng, Hanchao,Wen, Jian,Zhang, Duo,Raabe, Gerhard,Bolm, Carsten

, p. 2166 - 2169 (2016)

An efficient kinetic resolution of sulfoximines with enals was realized using chiral N-heterocyclic carbene (NHC) catalysts. The stereoselective amidation proceeds without additional acyl transfer agent. Both enantiomers of the sulfoximines can be obtaine

SMALL MOLECULE MODULATORS OF HEPATOCYTE GROWTH FACTOR (SCATTER FACTOR) ACTIVITY

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Page 92-93, (2010/02/07)

The present invention provides compounds having formula (I) and pharmaceutically acceptable derivatives thereof, wherein R1, R2 and B are as described generally and n classes and subclasses herein, and additionally provides pharmaceu

PALLADIUM-PROMOTED REACTION OF ALLYL TRIMETHYLSILYL ETHERS WITH ARYL IODIDES

Hirao, Toshikazu,Enda, Jun,Ohshiro, Yoshiki,Agawa, Toshio

, p. 403 - 406 (2007/10/02)

Allyl trimethylsilyl ether reacts with aryl iodides in the presence of palladium acetate and lithium chloride to afford selectively β-aryl (E)-α,β-unsaturated carbonyl compound.

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