114077-42-8

Basic information

• Product Name: Benzeneacetic acid, 2-hydroxy-a-(methoxymethylene)-, methyl ester, (E)-
• CAS NO: 114077-42-8
• Molecular Formula: C11H12O4
• Molecular Weight: 208.214
• Mol File: 114077-42-8.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: Benzeneacetic acid, 2-hydroxy-a-(methoxymethylene)-, methyl ester, (E)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzeneacetic acid, 2-hydroxy-a-(methoxymethylene)-, methyl ester, (E)-(114077-42-8)
• EPA Substance Registry System: Benzeneacetic acid, 2-hydroxy-a-(methoxymethylene)-, methyl ester, (E)-(114077-42-8)

Safety Data

• Hazardous Substances Data: 114077-42-8(Hazardous Substances Data)

Upstream product

• 103497-78-5 (E)-3-methoxy-2-(2-benzyloxyphenyl)acrylic acid methyl ester 
• 1634-04-4 tert-butyl methyl ether 
• 7440-05-3 palladium 
• 5788-17-0 methyl (2E)-3-methoxy-2-propenoate 
• 31575-75-4 2-bromophenyl benzyl ether 
• 95-56-7 2-hydroxybromobenzene 
• 24396-24-5 2-(dimethoxymethyl)phenol 
• 6832-16-2 methyl diazoacetate 
• 40525-65-3 2-benzyloxyphenylacetic acid methyl ester 
• 22446-37-3 methyl (2-hydroxyphenyl)acetate 
• 614-75-5 2-Hydroxyphenylacetic acid 
• 34846-90-7 methyl 3-methoxyprop-2-enoate 
• 40800-90-6 3-(α-methoxy)methylene benzofuran-2-(3H)-ketone 
• 124-41-4 sodium methylate 

Downstream Products

• 131860-97-4 (E)-methyl 2-[2-(6-chloropyrimidin-4-yloxy)phenyl]-3-methoxy-propenoate 
• 1266105-19-4 tert-butyl 6-(4-chloro-6-(2-((E)-1-(methoxycarbonyl)-2-methoxyvinyl)phenoxy)pyrimidin-2-yl)hexanoate 
• 215934-32-0 azoxystrobin 
• 114077-60-0 (E)-methyl 2-[2'-(5-nitropyridin-2-yloxy)phenyl]-3-methoxyacrylate 
• 114102-59-9 (E)-methyl 2-[2'-(4-chloropyrimidin-2-yloxy)phenyl]-3-methoxyacrylate 

Relevant articles and documents

Method for preparing alkoxy acrylate

The invention discloses a method for preparing an alkoxy acrylate. The method comprises that diazo ester and substituted acetal or ketal as raw materials undergo an alkenylation reaction in the presence of Lewis acid as a catalyst at 50-120 DEG C for 1-24h, then the solvent is drained through pumping and the product is subjected to column chromatography separation so that the alkoxy acrylate compound is obtained. The reaction raw materials and the catalyst are easily available and cheap, the synthesis process is simple, the synthesis cost is greatly reduced, the reaction conditions are mild, the yield is high, the industrialization is easy, the reaction raw materials and the catalyst are clean and non-toxic, and the environmental pollution is small.

Measuring method for measuring and using a kit or flagment autoantibody autoantibody or fragments thereof, and their azoxystrobin deriv., azoxystrobin

PROBLEM TO BE SOLVED: To provide a method for measuring the levels of an azoxystrobin as a fungicide left in samples such as of farm products or processed products. SOLUTION: An antibody specific to azoxystrobin is obtained by using a composite, as an immunogen, of an azoxystrobin derivative and a polymeric compound. The method for assaying azoxystrobin using such an antibody is provided. An assay kit therefor is prepared. COPYRIGHT: (C)2011,JPOandINPIT

Synthesis of novel quinazolinone derivatives with methyl (E)-2-(3-methoxy)acrylate moiety

A new series of quinazolinone derivatives with methyl (E)-2-(3-methoxy) acrylate moiety have been designed and synthesized. All target compounds had been identified by 1H NMR spectrum, IR spectrum and HR-MS (high resolution mass spectrum). Three target compounds (10a, 10e, 10h) were chosen to preliminarily test the antibacterial activities, the results showed that all three target compounds exhibited antibacterial activities against three bacterial strains (Proteobacteria, Salmonella, Colibacillus).