55784-07-1

Basic information

• Product Name: 4-(1-METHYLETHOXY)-BENZENEACETIC ACID
• Synonyms: 4-(1-METHYLETHOXY)-BENZENEACETIC ACID;BENZENEACETIC ACID, 4-(1-METHYLETHOXY)-;UKRORGSYN-BB BBV-106013
• CAS NO: 55784-07-1
• Molecular Formula: C₁₁H₁₄O₃
• Molecular Weight: 194.23
• Mol File: 55784-07-1.mol
• Article Data: 9

Chemical Properties

• Melting Point: 87 °C
• Boiling Point: 324.4±17.0 °C(Predicted)
• Appearance: /
• Density: 1.114±0.06 g/cm3(Predicted)
• PKA: 4.55±0.10(Predicted)
• CAS DataBase Reference: 4-(1-METHYLETHOXY)-BENZENEACETIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(1-METHYLETHOXY)-BENZENEACETIC ACID(55784-07-1)
• EPA Substance Registry System: 4-(1-METHYLETHOXY)-BENZENEACETIC ACID(55784-07-1)

Safety Data

• Hazardous Substances Data: 55784-07-1(Hazardous Substances Data)

Upstream product

• 156-38-7 4-hydroxyphenylacetate 
• 75-26-3 isopropyl bromide 
• 67-63-0 isopropyl alcohol 
• 29056-05-1 methyl 2-(4-isopropoxyphenyl)acetate 
• 55784-02-6 4-[(4-isopropoxy-phenyl)-thioacetyl]-morpholine 
• 14199-15-6 Methyl 4-hydroxyphenylacetate 

Downstream Products

• 86817-77-8 2-(p-isopropoxyphenyl)ethanol 
• 587870-58-4 α-(4-isopropoxyphenyl)-m,m-diisopropoxycinnamic acid 
• 587870-65-3 α-(p-isopropoxyphenyl)-p-isopropoxycinnamic acid 
• 639863-84-6 1-(isocyanatomethyl)-4-(propan-2-yloxy)benzene 
• 501-36-0 (E)-5-[2-4-(hydroxyphenyl)ethenyl]-1,3-benzenediol 
• 6628-41-7 α-(p-hydroxyphenyl)cinnamic acid 
• 148788-27-6 α-(p-hydroxyphenyl)-p-hydroxycinnamic acid 
• 61434-67-1 cis-resveratrol 
• 587870-59-5 cis-3,4',5-triisopropoxystilbene 
• 587870-67-5 (E)-1-(3,5-di-isopropoxyphenyl)-2-(4-isopropoxyphenyl)ethene 
• 86817-78-9 2-(p-isopropoxyphenyl)ethyl methyl ether 
• 1409950-43-1 1,7-difluoro-3-(4-isopropoxyphenyl)-6-methoxyisoquinoline 
• 1409950-45-3 (E)-3-(4-fluoro-3-methoxyphenyl)-2-(4-isopropoxyphenyl)acryloyl azide 
• 1409950-46-4 7-fluoro-3-(4-isopropoxyphenyl)-6-methoxyisoquinolin-1-ol 

Relevant articles and documents

Hepatitis C virus inhibitors

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Total synthesis of (±)-armepavines and (±)-nuciferines from (2-nitroethenyl)benzene derivatives

A concise route to armepavine 1 and nuciferine 2 and 3, which can be isolated from the leaves of Nelumbo nucifera (Nymphaceae), has been achieved in which the longest linear sequence is only six steps from commercially available benzaldehyde in 28%, 21%, and 20% overall yield, respectively. The key transformations in the synthesis are the radical cyclization of aryl bromide with Bu3SnH and the Pictet-Spengler reaction of N-substituted amine with aldehyde. Copyright Taylor & Francis Group, LLC.

A-[(E)-2-(5,6,7,8-TETRAHYDRO-5,5,8,8-TETRAMETHYL-2-NAPTHALENYL)-1-PROPENYL]BENZOIC ACID ANALOGS AND METHOD OF MANUFACTURE AND AND USE THEREOF

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