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Z-2-Methoxy-3-phenylthioacrylsaeure-O-methylester is a complex organic chemical compound with the molecular formula C12H12O4S. It is a derivative of acrylic acid, featuring a phenylthio group at the 3-position and a methoxy group at the 2-position. The compound is characterized by its conjugated double bond system, which is essential for its chemical reactivity and properties. It is commonly used in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. The compound is also known for its potential applications in materials science, particularly in the development of new polymers and other advanced materials. Its chemical structure and properties make it a valuable intermediate in organic synthesis, allowing for the creation of a wide range of products with diverse applications.

85477-33-4

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85477-33-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 85477-33-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,4,7 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85477-33:
(7*8)+(6*5)+(5*4)+(4*7)+(3*7)+(2*3)+(1*3)=164
164 % 10 = 4
So 85477-33-4 is a valid CAS Registry Number.

85477-33-4Downstream Products

85477-33-4Relevant academic research and scientific papers

O-Alkyl Thioates and Dithioates, 33. - Reactions of Phosphorus Ylides with Thiooxalates - A New Synthesis of α,β-Unsaturated O-Alkyl Thioates

Hartke, Klaus,Kumar, Arvind,Koester, Joachim

, p. 267 - 273 (2007/10/02)

The reaction of dimethyl tetrathiooxalate (1) with alkylidenetriphenylphosphoranes 2 leads to the formation of triphenylphosphane sulfide (3) and a complex mixture of unstable products; with the disubstituted phosphoranes 4a, b the 1,3-dithioles 5 and triphenylphosphane (6) were isolated.O,O-Dimethyl dithiooxalate (8) is transformed into α,β-unsaturated O-alkyl thioates 9 by thiocarbonyl olefination with 2 and 4.

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