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2-Propynoic acid, 3-(3-nitrophenyl)-, methyl ester is a chemical compound with the molecular formula C11H9NO4. It is an organic ester derived from 2-propynoic acid and 3-nitrophenol, featuring a methyl ester group attached to the carboxylic acid. 2-Propynoic acid, 3-(3-nitrophenyl)-, methyl ester is characterized by its unique structure, which includes a triple bond in the propynoic acid moiety and a nitro group on the phenyl ring. It is a yellowish crystalline solid and is soluble in organic solvents. Due to its reactivity and potential applications in the synthesis of various organic compounds, it is often used in research and development in the field of organic chemistry. However, it should be handled with care due to its potential toxicity and reactivity.

7515-22-2

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7515-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7515-22-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7515-22:
(6*7)+(5*5)+(4*1)+(3*5)+(2*2)+(1*2)=92
92 % 10 = 2
So 7515-22-2 is a valid CAS Registry Number.

7515-22-2Relevant academic research and scientific papers

Oxidant- and additive-free simple synthesis of 1,1,2-triiodostyrenes by one-pot decaroboxylative iodination of propiolic acids

Ghosh, Subhankar,Ghosh, Rajat,Chattopadhyay, Shital K.

supporting information, (2020/09/15)

A metal- and oxidant-free facile synthesis of a range of 1,1,2-triiodostryrene derivatives has been developed which utilizes a simple decarboxylative triiodination of propiolic acids using molecular iodine and sodium acetate in a one-pot manner. Electron-

Asymmetric Transfer Hydrogenation of gem-Difluorocyclopropenyl Esters: Access to Enantioenriched gem-Difluorocyclopropanes

Archambeau, Alexis,Cossy, Janine,Meyer, Christophe,Pierre, Hugo,Yamani, Khalil

supporting information, p. 18505 - 18509 (2020/08/27)

Catalytic enantioselective access to disubstituted functionalized gem-difluorocyclopropanes, which are emerging fluorinated motifs of interest in medicinal chemistry, was achieved through asymmetric transfer hydrogenation of gem-difluorocyclopropenyl este

Nitration of phenylpropiolic acid derivatives in HSO3F and reactions of vinyl type cations formed therefrom

Savechenkov,Rudenko,Vasil'ev

, p. 1633 - 1637 (2007/10/03)

Nitration of phenylpropiolic acid derivatives ArC≡CX (X=CN, CO 2Me) in HSO3F at -75...-50°C afforded mononitro compounds, for instance, m-O2NC6H4C≡CX. Vinyl type cations generated in HSO3F

Synthesis of 2-amino-6-phenyl-4H-pyran-4-ones

Morris,Wishka

, p. 43 - 46 (2007/10/02)

The treatment of a series of phenylacetylenic β-keto amides with methanesulfonic acid produces a high yielding intramolecular cyclization to the corresponding 2-amino-6-phenyl-4H-pyran-4-ones.

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