931-94-2

Usage

Uses

Used in Chemical Synthesis:
1,1-Dimethoxycyclopentane is used as a solvent for facilitating various chemical reactions, particularly in the synthesis of pharmaceuticals, agrochemicals, and other organic compounds. Its low reactivity and stability contribute to the controlled and efficient synthesis of target molecules.
Used in Industrial Processes:
In the industrial sector, 1,1-Dimethoxycyclopentane is utilized as a component in the production of various chemical products. Its favorable properties, such as low toxicity and stability, make it suitable for use in large-scale manufacturing processes.
Used in Laboratory Settings:
1,1-Dimethoxycyclopentane is employed as a solvent in laboratory research for conducting experiments and testing new chemical reactions. Its safety profile and compatibility with a wide range of reagents make it an ideal choice for scientific investigations.

InChI:InChI=1/C7H14O2/c1-8-7(9-2)5-3-4-6-7/h3-6H2,1-2H3

Upstream product

• 67-56-1 methanol 
• 17497-52-8 1-iodocyclopentene 
• 40648-08-6 2-methyl-1-iodo-1-cyclohexene 
• 120-92-3 cyclopentanone 
• 149-73-5 trimethyl orthoformate 

Downstream Products

• 92747-27-8 1-Methoxy-cyclopentanecarbonitrile 
• 112489-39-1 C₃₉H₄₂O₆ 
• 105119-26-4 (2R,3R)-2-(Benzyloxymethyl)-3-ethyl-1,4-dioxaspiro<4.4>nonane-2-carboxylic Acid 
• 105065-63-2 (2S,3R)-2-(Benzyloxymethyl)-3-ethyl-1,4-dioxaspiro<4.4>nonane-2-carboxylic Acid 
• 112489-39-1 C₃₉H₄₂O₆ 
• 106711-53-9 C₁₈H₂₄O₅ 
• 134311-79-8 C₁₈H₂₄O₅ 
• 132089-82-8 6-(4-chlorophenylthio)-9-(2,3-O-cyclopentylidene-β-D-ribofuranosyl)-9H-purine 
• 82281-61-6 Toluene-4-sulfonic acid (R)-2-((7R,8S)-9-isopropenyl-8-methyl-6,10-dioxa-spiro[4.5]dec-7-yl)-propyl ester 
• 4884-13-3 1,1’-dihydroperoxydi(cyclopentyl)peroxide 
• 132606-28-1 1,1-bis(hydroperoxy)cyclopentane 
• 120-92-3 cyclopentanone 
• 110950-03-3 (S)-2-((S)-1-Phenyl-allyl)-cyclopentanone 
• 110950-03-3 (R)-2-((S)-1-Phenyl-allyl)-cyclopentanone 

Relevant academic research and scientific papers

Catalytic asymmetric epoxidation

A compound and method for producing an enantiomerically enriched epoxide from an olefin using a chiral ketone and an oxidizing agent is disclosed.

Photochemistry of Alkyl Halides. 10. Vinyl Halides and Vinylidene Dihalides

The photobehavior of the acyclic vinyl iodide 2, the 1-iodocycloalkenes 11-14 and 39, the (halomethylene)cycloalkanes 45-48, and the (dihalomethylene)cyclohexanes 62-64 has been studied.Except for the dichloride 64, which exhibited only radical behavior, each of the halides afforded a mixture of ionic and radical products.The two bromides studied, 48 and 63, afforded lower ratios of ionic to radical products than the corresponding iodides 45 and 62.Irradiation of vinyl iodides was found to be a convenient and powerful method for the generation of vinyl cations, including the highly strained 1-cyclohexenyl and 1-cyclopentenyl cations and the unstabilized α-unsubstituted cations 51 and 54.The latter cations underwent rearrangement to the ring-expanded 1-cycloalkenyl cations 28 and 36, respectively.Lowering the temperature of the irradiation of iodides 13, 14, and 45 resulted in an increased ratio of ionic to radical products.However, iodide 47, which underwent principally fragmentation to enyne 61, showed little temperature effect.