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Methyl trans-2-hydroxy-3-methoxycarbonylcinnamate is a complex organic compound with the chemical formula C11H10O5. It is a derivative of cinnamic acid, featuring a hydroxyl group at the 2nd carbon and a methoxycarbonyl group at the 3rd carbon. methyl trans-2-hydroxy-3-methoxycarbonylcinnamate is characterized by its trans configuration, which refers to the geometric arrangement of the double bond, with the hydroxyl and methoxycarbonyl groups on opposite sides of the molecule. It is a white crystalline solid and is used in the synthesis of various pharmaceuticals and natural products due to its unique structural properties. The compound's chemical structure and functional groups make it a valuable intermediate in organic chemistry, particularly in the preparation of bioactive molecules and specialty chemicals.

2703-93-7

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2703-93-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2703-93-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,0 and 3 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 2703-93:
(6*2)+(5*7)+(4*0)+(3*3)+(2*9)+(1*3)=77
77 % 10 = 7
So 2703-93-7 is a valid CAS Registry Number.

2703-93-7Downstream Products

2703-93-7Relevant academic research and scientific papers

Convenient synthesis of a simple coumarin from salicylaldehyde and Wittig reagent. II: Synthesis of bromo- and methoxycarbonylcoumarins

Harayama,Nakatsuka,Nishioka,Murakami,Hayashida,Ishii

, p. 2170 - 2173 (1994)

Reaction of salicylaldehydes (1) with carbethoxymethylenetriphenylphosphorane in diethylaniline under reflux gave coumarins (3) in moderate to high yield except 3-methoxycarbonylsalicylaldehyde (1e). The substituent effects are discussed. A substituent at C6 on 1 usually facilitated the formation of the coumarin ring regardless of its electronic character.

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