74205-29-1

Basic information

• Product Name: 1-(3-METHOXY-PHENYL)-CYCLOPROPANECARBOXYLIC ACID
• Synonyms: 1-(3-METHOXY-PHENYL)-CYCLOPROPANECARBOXYLIC ACID;1-(3-Methoxyphenyl)cyclopropane-1-carboxylic acid;3-(1-Carboxycycloprop-1-yl)anisole, 1-Carboxy-1-(3-methoxyphenyl)cyclopropane
• CAS NO: 74205-29-1
• Molecular Formula: C₁₁H₁₂O₃
• Molecular Weight: 192.21118
• Product Categories: Carboxylic Acids;Phenyls & Phenyl-Het;Carboxylic Acids;Phenyls & Phenyl-Het
• Mol File: 74205-29-1.mol
• Article Data: 6

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-(3-METHOXY-PHENYL)-CYCLOPROPANECARBOXYLIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-METHOXY-PHENYL)-CYCLOPROPANECARBOXYLIC ACID(74205-29-1)
• EPA Substance Registry System: 1-(3-METHOXY-PHENYL)-CYCLOPROPANECARBOXYLIC ACID(74205-29-1)

Safety Data

• Hazardous Substances Data: 74205-29-1(Hazardous Substances Data)

Usage

General Description

1-(3-Methoxy-phenyl)-cyclopropanecarboxylic acid is a chemical compound with the molecular formula C12H12O3. It is a carboxylic acid derivative that contains a cyclopropane ring and a phenyl group with a methoxy substituent. 1-(3-METHOXY-PHENYL)-CYCLOPROPANECARBOXYLIC ACID is commonly used as a starting material in the synthesis of various pharmaceuticals and other organic compounds. It may also exhibit biological activities and potential therapeutic properties due to its structural features. Additionally, it is important to handle this compound with care and follow proper safety measures when working with it in laboratory settings.

Upstream product

• 74205-01-9 1-(3-methoxyphenyl)cyclopropanecarbonitrile 
• 19924-43-7 3-methoxyphenylacetonitrile 

Downstream Products

• 1083168-98-2 N-(6'-methoxy-3,5'-dimethyl-2,3'-bipyridin-6-yl)-1-(3-methoxyphenyl)cyclopropanecarboxamide 
• 1083168-58-4 1-(3-methoxyphenyl)-N-(5-methyl-6-(5-methyl-6-oxo-1,6-dihydropyridin-3-yl)pyridin-2-yl)cyclopropanecarboxamide 
• 1624333-37-4 (1-(3-methoxyphenyl)cyclopropyl)(trifluoromethyl)sulfane 
• 1268444-73-0 (4R)-4-[(2-chlorophenyl)sulfonyl]-N-(1-cyanocyclopropyl)-1-{[1-(3-methoxyphenyl)cyclopropyl]carbonyl}-L-prolinamide 
• 61492-22-6 (2S,5R,6R)-6-{[1-(3-Methoxy-phenyl)-cyclopropanecarbonyl]-amino}-3,3-dimethyl-7-oxo-4-thia-1-aza-bicyclo[3.2.0]heptane-2-carboxylic acid 
• 108098-17-5 (6R,7R)-7-{[1-(3-Methoxy-phenyl)-cyclopropanecarbonyl]-amino}-3-methyl-8-oxo-5-thia-1-aza-bicyclo[4.2.0]oct-2-ene-2-carboxylic acid 
• 63201-08-1 C₁₁H₁₁ClO₂ 

Relevant articles and documents

Chiral Bidentate Boryl Ligand Enabled Iridium-Catalyzed Enantioselective C(sp3)-H Borylation of Cyclopropanes

We herein report an Ir-catalyzed enantioselective C(sp3)-H borylation of cyclopropanecarboxamides using a chiral bidentate boryl ligand for the first time. A variety of substrates with α-quaternary carbon centers could be compatible in this reaction to provide β-borylated products with good to excellent enantioselectivities. We have also demonstrated that the borylated products can be used as versatile precursors engaging in stereospecific transformations of C-B bonds, including the synthesis of a bioactive compound Levomilnacipran.

Rhodium-Catalyzed Enantioselective Silylation of Cyclopropyl C?H Bonds

Hydrosilyl ethers, generated in situ by the dehydrogenative silylation of cyclopropylmethanols with diethylsilane, undergo asymmetric, intramolecular silylation of cyclopropyl C?H bonds in high yields and with high enantiomeric excesses in the presence of

SUBSTITUTED ARYLPYRAZOLOPYRIDINES AND SALTS THEREOF, PHARMACEUTICAL COMPOSITIONS COMPRISING SAME, METHODS OF PREPARING SAME AND USES OF SAME

The invention relates to substituted arylpyrazolopyridines according to the general formula (I) : in which A, B, D, E, Ra, R1, R2, R3, R4, R5 and q are as defined in the claims, and salts t