893751-08-1

Basic information

• Product Name: METHYL 2-(4-FLUOROPHENYL)CYCLOPROPANECARBOXYLATE
• Synonyms: METHYL 2-(4-FLUOROPHENYL)CYCLOPROPANECARBOXYLATE
• CAS NO: 893751-08-1
• Molecular Formula: C11H11FO2
• Molecular Weight: 194.2
• Mol File: 893751-08-1.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: METHYL 2-(4-FLUOROPHENYL)CYCLOPROPANECARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL 2-(4-FLUOROPHENYL)CYCLOPROPANECARBOXYLATE(893751-08-1)
• EPA Substance Registry System: METHYL 2-(4-FLUOROPHENYL)CYCLOPROPANECARBOXYLATE(893751-08-1)

Safety Data

• Hazardous Substances Data: 893751-08-1(Hazardous Substances Data)

Upstream product

• 186581-53-3 diazomethane 
• 96426-60-7 methyl (2E)-3-(4-fluorophenyl)-2-propenoate 
• 459-32-5 (E)-4-fluorocinnamic acid 
• 352-34-1 4-fluoro-1-iodobenzene 
• 67-56-1 methanol 
• 515179-19-8 (±)-trans-2-(4-fluorophenyl)cyclopropane-1-carboxylic acid 
• 405-99-2 para-fluorostyrene 
• 6832-16-2 methyl diazoacetate 

Downstream Products

• 515179-19-8 2-(4-fluorophenyl)cyclopropanecarboxylic acid 
• 161711-27-9 (1R,2R)-2-(4-fluorophenyl)cyclopropanecarboxylic acid 
• 1314323-96-0 (1R,2S)-tert-butyl 2-(4-fluorophenyl)cyclopropylcarbamate 
• 113516-71-5 (1R,2S)-2-(4-fluorophenyl)cyclopropan-1-amine 

Relevant articles and documents

Donor-Acceptor Bicyclopropyls as 1,6-Zwitterionic Intermediates: Synthesis and Reactions with 4-Phenyl-1,2,4-triazoline-3,5-dione and Terminal Acetylenes

The bicyclopropyl system activated by incorporation of donor and acceptor groups in the presence of Lewis acids was used as a synthetic equivalent of 1,6-zwitterions. Opening of both cyclopropane rings in 2′-aryl-1,1′-bicyclopropyl-2,2-dicarboxylates (D-A bicyclopropyl, ABCDs) in the presence of GaI3 + Bu4N+GaI4- results in 5-iodo-5-arylpent-2-enylmalonates as products of HI formal 1,6-addition to the bicyclopropyl system. The use of GaCl3 or GaBr3 as a Lewis acid and terminal aryl or alkyl acetylenes as 1,6-zwitterion interceptors allows the alkyl substituent to be grown to give the corresponding acyclic 7-chloro(bromo)-hepta-2,6-dienylmalonates. The reaction of ABCDs with 4-phenyl-1,2,4-triazoline-3,5-dione (PTAD) catalyzed by Yb(OTf)3 also results in the opening of both cyclopropane rings. The reaction products are tetrahydropyridazine derivatives - (7,9-dioxo-1,6,8-triazabicyclo[4.3.0]non-3-en-2-ylmethyl)malonates - containing one more PTAD moiety in the malonyl group.

TRIAZOLOPYRIDINE ETHER DERIVATIVES AND THEIR USE IN NEUROLOGICAL AND PYSCHIATRIC DISORDERS

The disclosure generally relates to compounds of formula I, including their salts, as well as compositions and methods of using the compounds. The compounds modulate the mGluR2 receptor and may be useful for the treatment of various disorders of the central nervous system.

Novel trans-2-aryl-cyclopropylamine analogues as potent and selective dipeptidyl peptidase IV inhibitors

A series of trans-2-aryl-cyclopropylamine derived compounds were synthesized and evaluated their biological activities against DPP-IV. The structure-activity relationships (SAR) led to the discovery of novel series of DPP-IV inhibitors, having IC50 values of 100 nM with excellent selectivity over the closely related enzymes, DPP8, DPP-II and FAP. The studies identified a potent and selective DPP-IV inhibitor 24b, which exhibited the ability to both significantly inhibit plasma DPP-IV activity in rats and improve glucose tolerance in lean mice and diet induced obese mice.