426225-93-6

Basic information

• Product Name: METHYL (1R,4R)-4-(HYDROXYMETHYL)CYCLOPENT-2-ENE-1-CARBOXYLATE
• Synonyms: METHYL (1R,4R)-4-(HYDROXYMETHYL)CYCLOPENT-2-ENE-1-CARBOXYLATE
• CAS NO: 426225-93-6
• Molecular Formula: C₈H₁₂O₃
• Molecular Weight: 156.17908
• Mol File: 426225-93-6.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 234.2±23.0 °C(Predicted)
• Appearance: /
• Density: 1.143±0.06 g/cm3(Predicted)
• PKA: 14.39±0.40(Predicted)
• CAS DataBase Reference: METHYL (1R,4R)-4-(HYDROXYMETHYL)CYCLOPENT-2-ENE-1-CARBOXYLATE(CAS DataBase Reference)
• NIST Chemistry Reference: METHYL (1R,4R)-4-(HYDROXYMETHYL)CYCLOPENT-2-ENE-1-CARBOXYLATE(426225-93-6)
• EPA Substance Registry System: METHYL (1R,4R)-4-(HYDROXYMETHYL)CYCLOPENT-2-ENE-1-CARBOXYLATE(426225-93-6)

Safety Data

• Hazardous Substances Data: 426225-93-6(Hazardous Substances Data)

Upstream product

• 426225-92-5 (1S,3R)-1-(2-dimethylmalonyl)-3-triphenylmethoxy-4-cyclopentene 
• 426225-90-3 (1S,3R)-1-Hydroxy-3-triphenylmethoxy-4-cyclopentene 
• 426225-91-4 (1R,3R)-1-chloro-3-triphenylmethoxy-4-cyclopentene 
• 115074-49-2 (1R,4S)-4-[(tert-butyldimethylsilyl)oxy]-2-cyclopentene-1-yl acetate 
• 120520-91-4 (1R,4S)-4-(tert-butyldimethylsilyloxy)cyclopent-2-enol 
• 60410-16-4 (1R,4S)-4-hydroxy-2-cyclopentene-1-yl acetate 
• 660439-53-2 ((1R,4R)-4-Trityloxy-cyclopent-2-enyl)-acetic acid methyl ester 
• 80-73-9 1,3-dimethyl-2-imidazolidinone 
• 10581-12-1 tetramethyl ammonium acetate 

Downstream Products

• 1211-29-6 methyl (2-(2-pent-2Z-enyl)-3-oxocyclopentyl)acetate 
• 128820-28-0 (1S,5S,8R)-8-<(2'Z)-pent-2'-enyl>-2-oxybicyclo<3.2.1>octan-3-on 
• 866392-85-0 Benzoic acid (1S,4R)-4-methoxycarbonylmethyl-cyclopent-2-enyl ester 

Relevant articles and documents

Regulation of type 5 adenylyl cyclase for treatment of neurodegenerative and cardiac diseases

The invention concerns pharmaceutical compositions that contain a compound or compounds that can effectively regulate the activity of Type 5 Adenylyl Cyclase and methods for treatment of neurological diseases and disorders, as well as motor function loss

Methyl-jasmonat: Ein kurzer Weg zum Naturstoff und seinem unnatuerlichen Enantiomer via Palladium(0)-induzierte, enantiodivergente Alkylierung von Cyclopent-2-en-1,3-diol-Derivaten

Palladium-catalyzed alkylation of cyclopent-2-ene-1,2-diol derivatives like 2 is a useful method for enantiodivergent functionalization, resulting both enantiomeric series of chiral building blocks.The chiral building blocks 3 and 13 can be transformed to methyl-jasmonate (1) and its unnatural enantiomer ent-1, recent statement that 1 has no odour at all and that "methyl-jasmonate's" fragrance is actually due to its cis-isomer ent-11 has been confirmed also for the enantiomeric series.