51264-73-4

Basic information

• Product Name: ethyl 2-(4-formylphenoxy)propionate
• Synonyms: ethyl 2-(4-formylphenoxy)propionate;2-(4-Formylphenoxy)propionic acid ethyl ester
• CAS NO: 51264-73-4
• Molecular Formula: C₁₂H₁₄O₄
• Molecular Weight: 222.23716
• EINECS: 257-095-9
• Mol File: 51264-73-4.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 335.9°Cat760mmHg
• Flash Point: 147.5°C
• Appearance: /
• Density: 1.139g/cm³
• Vapor Pressure: 0.000116mmHg at 25°C
• Refractive Index: 1.527
• CAS DataBase Reference: ethyl 2-(4-formylphenoxy)propionate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-(4-formylphenoxy)propionate(51264-73-4)
• EPA Substance Registry System: ethyl 2-(4-formylphenoxy)propionate(51264-73-4)

Safety Data

• Hazardous Substances Data: 51264-73-4(Hazardous Substances Data)

Usage

InChI:InChI=1/C12H14O4/c1-3-15-12(14)9(2)16-11-6-4-10(8-13)5-7-11/h4-9H,3H2,1-2H3

Upstream product

• 123-08-0 4-hydroxy-benzaldehyde 
• 535-11-5 Ethyl 2-bromopropionate 
• 58742-64-6 ethyl l-2-((methylsulfonyl)oxy)propionate 
• 68-12-2 N,N-dimethyl-formamide 
• 535-13-7 2-chloro-propanoic acid, ethyl ester 

Downstream Products

• 70044-37-0 Ethyl-2-<4-(hydroxymethyl)phenoxy>propionat 
• 1361043-99-3 ethyl 2-(4-(bis(2-methyl-1H-indol-3-yl)methyl)phenoxy)propanoate 
• 1361043-98-2 ethyl 2-(4-(bis(1-methyl-1H-indol-3-yl)methyl)phenoxy)propanoate 
• 1361044-01-0 ethyl 2-(4-(bis(1,2-dimethyl-1H-indol-3-yl)methyl)phenoxy)propanoate 
• 1361044-00-9 ethyl 2-(4-(bis(1-ethyl-1H-indol-3-yl)methyl)phenoxy)propanoate 
• 65343-67-1 ethyl 2-(4-hydroxyphenoxy)propanoate 

Relevant articles and documents

Microwave-assisted efficient synthesis of pyrazole-fibrate derivatives as stimulators of glucose uptake in skeletal muscle cells

The design and synthesis of a series of pyrazolo[3,4-d]pyrimidinones containing fibrate side chains have been accomplished by utilizing the concept of molecular hybridization. All the synthesized compounds were evaluated for the glucose uptake stimulatory effect in L6 rat skeletal muscle cells. Four compounds (3f, 3g, 3j and 3q) were found to show significant stimulation of glucose uptake. Further these four compounds have been examined for their Glut4 translocation stimulatory effect in L6-Glut4myc myotubes. Compound 3q was found to exert maximum increase in GLUT4myc translocation.

HYPOPHOSPHOROUS ACID DERIVATIVES HAVING ANTIHYPERALGIC ACTIVITY AND BIOLOGICAL APPLICATIONS THEREOF

The invention relates to hypophosphorous acid derivatives of formula (I) wherein - X is H or OH, - R represents one or several radicals R1-R5, identical or different, two of R1-R5 optionally occupying the same position on the phenyl group, one to four of R1-R5 being H and the others being selected in the group comprising - 0-(CH2)n-COOH; - S-(CH2)n-COOH; -NH-(CH2)n-COOH; - 0-(CH,R') -COOH; -O- (CH2)n-OH; OR', -R' being a C1 -C3 alkyl radical;-OH; --COOH; halogen, particularly -F, - CI, -Br, -I, -CF3; -OCF3; -N02; -CH=CH-COOH; - -(CH2)n-COOH; O - (CH2)n- P03H2; O - (CF2)n- P03H2; O - (CH2)n- S03H; O - (CH2)n- CONHOH; O - (CH2)n-tetrazol; O - (CH2)n-hydroxyisoxazol - n = 1 to 5, preferably 1-3; said hypophosrous acid derivatives being diastereoisomers or enantiomers.