1857-57-4

Basic information

• Product Name: 3-(3-BroMo-4-Methoxyphenyl)propionic acid, 96%
• Synonyms: 3-(3-BroMo-4-Methoxyphenyl)propionic acid, 96%
• CAS NO: 1857-57-4
• Molecular Formula: C₁₀H₁₁BrO₃
• Molecular Weight: 259.09654
• Mol File: 1857-57-4.mol
• Article Data: 7

Chemical Properties

• Melting Point: 96-100℃
• Boiling Point: 371.3 °C at 760 mmHg
• Flash Point: 178.3 °C
• Appearance: /
• Density: 1.492 g/cm³
• PKA: 4.63±0.10(Predicted)
• CAS DataBase Reference: 3-(3-BroMo-4-Methoxyphenyl)propionic acid, 96%(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(3-BroMo-4-Methoxyphenyl)propionic acid, 96%(1857-57-4)
• EPA Substance Registry System: 3-(3-BroMo-4-Methoxyphenyl)propionic acid, 96%(1857-57-4)

Safety Data

• Hazardous Substances Data: 1857-57-4(Hazardous Substances Data)

Usage

General Description

3-(3-Bromo-4-Methoxyphenyl)propionic acid, 96% is a chemical compound with a high level of purity. It is classified as an organic compound and is commonly used in research and laboratory settings. This chemical is a propionic acid derivative with a bromo and methoxy group attached to the phenyl ring. It is commonly used in pharmaceutical and medicinal chemistry for the synthesis of various organic compounds. This chemical is known for its high purity, making it a valuable resource for researchers and scientists in the field of organic chemistry.

Upstream product

• 1929-29-9 3-(4-methoxyphenyl)propanoic acid 
• 53375-71-6 ethyl 3-(3-bromo-4-methoxyphenyl)propanoate 
• 15823-04-8 methyl 3-(4-methoxyphenyl)propionate 
• 288310-70-3 3-(3-bromo-4-methoxyphenyl)-propionic acid methyl ester 
• 60553-38-0 methyl 3-(3-bromo-4-hydroxy-phenyl)propionate 

Downstream Products

• 1354834-15-3 3-(3-bromo-4-methoxyphenyl)-N-methoxy-N-methylpropanamide 
• 1354834-20-0 (E)-1-(3-bromo-4-methoxyphenyl)-7-(3-hydroxy-4-methoxyphenyl)hept-6-en-3-one 
• 1354834-19-7 (E)-7-(4-(benzyloxy)-3-methoxyphenyl)-1-(3-bromo-4-methoxyphenyl)hept-6-en-3-one 
• 1354834-17-5 1-(3-bromo-4-methoxyphenyl)hept-6-en-3-one 
• 1330753-35-9 1-(3-bromo-4-methoxyphenyl)-7-(3-hydroxy-4-methoxyphenyl)heptan-3-one 
• 1330753-47-3 1-(3-bromo-4-methoxyphenyl)-7-(3-methoxy-4-hydroxyphenyl)heptan-3-one 
• 187872-11-3 5-bromo-6-methoxy-2,3-dihydro-1H-inden-1-one 
• 590417-77-9 methyl 3-(3-bromo-4-methoxy-5-nitrophenyl)Propionate 
• 20146-10-5 3-(3-bromo-4-hydroxyphenyl)propanoic acid 
• 288311-04-6 5-(3-bromo-4-methoxy-phenyl)-3-oxo-2-(triphenyl-λ⁵-phosphanylidene)-pentanenitrile 
• 288310-71-4 4-(3-bromo-4-methoxy-phenyl)-1,1,1-trifluoro-bytan-2-one 
• 288311-05-7 methyl 4-(3-bromo-4-methoxy-phenyl)-2-oxo-butyrate 
• 288310-70-3 3-(3-bromo-4-methoxyphenyl)-propionic acid methyl ester 
• 946-62-3 3-(3-bromo-4-methoxyphenyl)propanoyl chloride 

Relevant articles and documents

Synthesis and evaluation of macrocyclic diarylether heptanoid natural products and their analogs

The macrocyclic diarylether heptanoid (MDEH) natural products have been used in folk medicine for centuries. MDEHs are reported to exert anti-tumor properties by inhibiting the activation of NF-κB. Here we report the synthesis of a small MDEH library (first reported synthesis of racemic platycarynol) using a Grubbs cross metathesis/Ullmann cyclization strategy. Evaluation of the library led to the identification of MDEH 9b which sensitizes pancreatic cancer cells to gemcitabine mediated growth inhibition and apoptosis.

INDENONCARBOXYLIC ACIDS DERIVATIVES AND THEIR USE FOR THE TREATMENT OF AND PREVENTING DIABETES AND DYSLIPIDAEMIA

The present invention relates to a compound of the formula ((I): in which: n is an integer chosen from 1, 2 and 3; Y represents O; N-OR9, in which R9represents H or a saturated hydrocarbon-based aliphatic group; CR10R

Synthesis of α-keto esters and amides via oxidative cleavage of cyanoketophosphoranes by dimethyldioxirane

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