56951-00-9 Usage
Description
(3Z)-3-(ethoxy-hydroxy-methylidene)-4-methyl-pyridine-2,6-dione is a pyridine-2,6-dione derivative with a molecular formula of C9H9NO4. It features an ethoxy and hydroxy functional group, which contributes to its unique chemical structure. (3Z)-3-(ethoxy-hydroxy-methylidene)-4-methyl-pyridine-2,6-dione has potential applications in the pharmaceutical and industrial sectors and may serve as a building block in organic synthesis.
Uses
Used in Pharmaceutical Industry:
(3Z)-3-(ethoxy-hydroxy-methylidene)-4-methyl-pyridine-2,6-dione is used as a chemical intermediate for the synthesis of various pharmaceutical compounds. Its unique structure allows it to be a potential candidate for the development of new drugs.
Used in Industrial Applications:
In the industrial sector, (3Z)-3-(ethoxy-hydroxy-methylidene)-4-methyl-pyridine-2,6-dione can be utilized as a building block in the synthesis of various organic compounds. Its versatility in chemical reactions makes it a valuable component in the creation of new materials and products.
Used in Organic Synthesis:
(3Z)-3-(ethoxy-hydroxy-methylidene)-4-methyl-pyridine-2,6-dione is used as a key component in organic synthesis, where it can be further modified or combined with other compounds to create new molecules with specific properties and applications. Its unique structure and functional groups make it a promising candidate for the development of novel organic compounds.
Check Digit Verification of cas no
The CAS Registry Mumber 56951-00-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,9,5 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 56951-00:
(7*5)+(6*6)+(5*9)+(4*5)+(3*1)+(2*0)+(1*0)=139
139 % 10 = 9
So 56951-00-9 is a valid CAS Registry Number.
InChI:InChI=1/C9H11NO4/c1-3-14-9(13)7-5(2)4-6(11)10-8(7)12/h4,13H,3H2,1-2H3,(H,10,11,12)/b9-7-
56951-00-9Relevant articles and documents
Reaction of β-Aminocrotonamide with Dibasic Acid Derivatives
Sato, Masayuki,Ogasawara, Hiromichi,Kato, Tetsuzo
, p. 87 - 91 (2007/10/02)
Reaction of β-aminocrotonamide (1) with succinic anhydride gave β-succinamidocrotonamide (3a), which was treated with base to cyclize to 3,4-dihydro-6-methyl-4-oxo-2-pyrimidinepropanoic acid (4a).Similarly, pyrimidinepentanoic acid derivative 4b was prepared from compound 1 and glutaric anhydride.Reaction of compound 1 with dimethyl succinate in the presence of sodium methoxide gave the pyrimidine derivative 4a.Similar reaction of compound 1 with glutarate, adipate, and phthalate gave the corresponding pyrimidines 4b, 4c and 4d, while reaction of compound 1 with malon ate gave 2-hydroxypyridine derivative 11 and dimethylpyrimidinone 4e.Reaction of dimethyl fumarate with compound 1 in the presence of methoxide gave a poor yield of pyrrolopyridine derivative 13.
