58026-12-3

Basic information

• Product Name: dimethyl formylsuccinate
• Synonyms: dimethyl formylsuccinate;2-Formylsuccinic acid dimethyl ester;Einecs 261-075-5
• CAS NO: 58026-12-3
• Molecular Formula: C₇H₁₀O₅
• Molecular Weight: 174.1513
• EINECS: 261-075-5
• Mol File: 58026-12-3.mol
• Article Data: 14

Chemical Properties

• Boiling Point: 247.1°Cat760mmHg
• Flash Point: 103.7°C
• Appearance: /
• Density: 1.17g/cm³
• Vapor Pressure: 0.0261mmHg at 25°C
• Refractive Index: 1.426
• PKA: 6.75±0.59(Predicted)
• CAS DataBase Reference: dimethyl formylsuccinate(CAS DataBase Reference)
• NIST Chemistry Reference: dimethyl formylsuccinate(58026-12-3)
• EPA Substance Registry System: dimethyl formylsuccinate(58026-12-3)

Safety Data

• Hazardous Substances Data: 58026-12-3(Hazardous Substances Data)

Usage

InChI:InChI=1/C7H10O5/c1-11-6(9)3-5(4-8)7(10)12-2/h4-5H,3H2,1-2H3

Upstream product

• 106-65-0 Dimethyl succinate 
• 201230-82-2 carbon monoxide 
• 107-31-3 Methyl formate 
• 109-94-4 formic acid ethyl ester 

Downstream Products

• 5204-91-1 methyl 5-oxotetrahydro-3-furancarboxylate 
• 85301-38-8 isocytosin-5-ylacetic acid 
• 6482-32-2 2-(hydroxymethyl)butane-1,4-diol 
• 20299-15-4 2-thio-5-<(methylcarboxy)methyl>uridine 
• 1613530-52-1 C₁₈H₂₂N₂O₁₀S 
• 29571-40-2 5-methoxycarbonylmethyl-2-thiouracil 
• 29571-39-9 ethyl 2-(4-oxo-2-thioxo-1,2,3,4-tetrahydropyrimidin-5-yl)acetate 
• 860426-55-7 {[benzyl-(1-methoxycarbonyl-ethyl)-amino]-methylene}-succinic acid dimethyl ester 
• 857754-17-7 N-benzyl-N-(2,3-bis-methoxycarbonyl-propenyl)-phenylalanine methyl ester 

Relevant articles and documents

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NOVEL QUINOLINECARBOXYLIC ACID DERIVATIVE AND MEDICAMENT CONTAINING THE SAME

PROBLEM TO BE SOLVED: To provide a compound that inhibits the formation of amyloid fibrils, an amyloid fibrils formation inhibitor containing the compound, and therapeutic or preventive agents for neurodegenerative diseases. SOLUTION: The present invention provides a compound represented by formula (I). [X is -(CH2)n-; n is an integer of 0-3; Y is a single bond or a divalent linking group such as an alkyl group; Ar is a substituted/unsubstituted phenyl group or pyridyl group; R1 is a substituted/unsubstituted alkyl group; Ar and R1, Ar and Y or R1 and Y may form a ring together; R2-R4 independently represent H, a C1-20 alkyl group or the like]. SELECTED DRAWING: None COPYRIGHT: (C)2019,JPO&INPIT

ALTERNATIVE NUCLEIC ACID MOLECULES AND USES THEREOF

The present disclosure provides alternative nucleosides, nucleotides, and nucleic acids, and methods of using them.