220235-68-7

Basic information

• Product Name: Propanoic acid, 2-[(4-methoxyphenyl)methoxy]-, methyl ester, (2S)-
• CAS NO: 220235-68-7
• Molecular Formula: C12H16O4
• Molecular Weight: 224.257
• Mol File: 220235-68-7.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Propanoic acid, 2-[(4-methoxyphenyl)methoxy]-, methyl ester, (2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: Propanoic acid, 2-[(4-methoxyphenyl)methoxy]-, methyl ester, (2S)-(220235-68-7)
• EPA Substance Registry System: Propanoic acid, 2-[(4-methoxyphenyl)methoxy]-, methyl ester, (2S)-(220235-68-7)

Safety Data

• Hazardous Substances Data: 220235-68-7(Hazardous Substances Data)

Upstream product

• 27871-49-4 (S)-Methyl lactate 
• 824-94-2 p-methoxybenzyl chloride 
• 105-13-5 4-Methoxybenzyl alcohol 
• 89238-99-3 O-(4-methoxybenzyl)-trichloroacetimidate 
• 220235-77-8 4-methoxybenzyl-2-pyridylthio carbonate 

Downstream Products

• 861902-93-4 (S)-N-methoxy-2-((4-methoxybenzyl)oxy)-N-methylpropanamide 
• 1058681-56-3 (S)-3-((4-methoxybenzyl)oxy)butan-2-one 
• 1058681-93-8 (2S,5S)-5-hydroxy-2-((4-methoxybenzyl)oxy)-6-methylhept-6-en-3-one 
• 1415121-62-8 (2S,5R)-5-hydroxy-2-((4-methoxybenzyl)oxy)-6-methylhept-6-en-3-one 
• 1058681-85-8 (2S,5S)-5-hydroxy-2-((4-methoxybenzyl)oxy)-6-methylheptan-3-one 
• 1415121-54-8 (2S,5R)-5-hydroxy-2-((4-methoxybenzyl)oxy)-6-methylheptan-3-one 
• 1415121-60-6 (2S,5S)-5-hydroxy-2-((4-methoxybenzyl)oxy)heptan-3-one 
• 332837-95-3 (3R,4S)-4-((E)-2-Iodo-propenyl)-1-[(S)-2-(4-methoxy-benzyloxy)-propionyl]-3-methyl-azetidin-2-one 
• 332837-94-2 (S)-2-(4-methoxybenzyloxy)propanoyl chloride 
• 370094-70-5 (4S,5S)-4-(triethyl)silyloxy-5-(4-methoxybenzyloxy)-1-hexanol 
• 321522-41-2 (4S,5S)-4-(triethyl)silyloxy-5-(4-methoxybenzyloxy)-1-hexene 
• 370094-48-7 (4S,5S)-4-(triethyl)silyloxy-5-(4-methoxybenzyloxy)-1-hexanal 

Relevant articles and documents

INHIBITORS OF INDOLEAMINE 2,3-DIOXYGENASE AND METHODS OF THEIR USE

The present invention provides a compound of formula (II): an inhibitor of indoleamine 2,3-dioxygenase (IDO), which may be used as medicaments for the treatment of proliferative disorders, such as cancer, viral infections and/or autoimmune diseases. Its prodrugs are disclosed.

Polyoxygenated Tertiary Alcohols: A Kiyooka Approach

A Kiyooka aldol approach for the stereoselective synthesis of tertiary alcohols is presented. This approach allows for the incorporation of different substituents at all three remaining positions at the chiral center bearing the tertiary alcohol. To demon

Structure determination and total synthesis of (+)-16-hydroxy-16,22- dihydroapparicine

Herein, we describe the first asymmetric total synthesis and determination of the relative and absolute stereochemistry of naturally occurring 16-hydroxy-16,22-dihydroapparicine. The key steps include 1) a novel phosphinimine-mediated cascade reaction to