88335-96-0

Basic information

• Product Name: 1,2-Cyclopropanedicarboxylic acid, monomethyl ester, (1S,2S)-
• CAS NO: 88335-96-0
• Molecular Formula: C6H8O4
• Molecular Weight: 144.127
• Mol File: 88335-96-0.mol
• Article Data: 13

Chemical Properties

• CAS DataBase Reference: 1,2-Cyclopropanedicarboxylic acid, monomethyl ester, (1S,2S)-(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Cyclopropanedicarboxylic acid, monomethyl ester, (1S,2S)-(88335-96-0)
• EPA Substance Registry System: 1,2-Cyclopropanedicarboxylic acid, monomethyl ester, (1S,2S)-(88335-96-0)

Safety Data

• Hazardous Substances Data: 88335-96-0(Hazardous Substances Data)

Upstream product

• 826-34-6 dimethyl cis-cyclopropane-1,2-dicarboxylate 
• 5861-31-4 methyl trans-2-phenylcyclopropanecarboxylate 
• 3999-55-1 diethyl trans-cyclopropane-1,2-dicarboxylate 
• 826-35-7 dimethyl trans-1,2-cyclopropanedicarboxylate 
• 67-56-1 methanol 
• 5617-74-3 cis-1,2-cyclopropanedicarboxylic acid anhydride 
• 5617-74-3 3-oxabicyclo[3.1.0]hexane-2,4-dione 
• 124-41-4 sodium methylate 
• 58616-95-8 trans-1,2-cyclopropanedicarboxylic acid 

Downstream Products

• 1142214-36-5 (1S,2S)-2-(benzo[d]oxazol-2-yl)cyclopropane-1-carboxylic acid 
• 16205-67-7 dimethyl (1S,2S)-cyclopropane-1,2-dicarboxylate 
• 781658-85-3 1,2;3,4-(di-O-isopropylidene)-6-O-α-D-galactopyranosyl (1S,2S)-2-(3,4-dichlorobenzoyl)-cyclopropane-1-carboxylate 

Relevant articles and documents

CYCLOPROPANECARBOXYLIC ACID GPR120 MODULATORS

The present invention provides compounds of Formula (I): or a stereoisomer, or a pharmaceutically acceptable salt thereof, wherein all of the variables are as defined herein. These compounds are GPR120 G protein coupled receptor modulators which may be used as medicaments

AROMATIC RING COMPOUND

The present invention provides an aromatic ring compound having a melanin-concentrating hormone receptor antagonistic action and useful as an agent for the prophylaxis or treatment of obesity and the like. The present invention relates to a compound represented by the formula wherein each symbol as defined in the specification, or a salt thereof.

Highly enantioselective desymmetrization of meso anhydrides by a bifunctional thiourea-based organocatalyst at low catalyst loadings and room temperature

(Chemical Equation Presented) Bifunctional (thio)urea-based cinchona alkaloid derivatives have been shown to promote highly efficient enantioselective desymmetrization reactions of meso anhydrides. The most selective of these catalysts is capable of the enantioselective methanolysis of succinic and glutaric anhydride derivatives to form hemiester products with >90% yield and enantiomeric excess at 1 mol % loading and ambient temperature.