931-94-2

Basic information

• Product Name: 1,1-DIMETHOXYCYCLOPENTANE
• Synonyms: CYCLOPENTANONE DIMETHYLKETAL;1,1-DIMETHOXYCYCLOPENTANE;1,1-Dimethoxypentane;Dimethoxypentane;Cyclopentanone dimethyl acetal
• CAS NO: 931-94-2
• Molecular Formula: C₇H₁₄O₂
• Molecular Weight: 130.18
• Mol File: 931-94-2.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 140 °C
• Flash Point: 27.1°C
• Appearance: /
• Density: 0.95
• Vapor Pressure: 9.25mmHg at 25°C
• Refractive Index: 1.4240-1.4300
• CAS DataBase Reference: 1,1-DIMETHOXYCYCLOPENTANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-DIMETHOXYCYCLOPENTANE(931-94-2)
• EPA Substance Registry System: 1,1-DIMETHOXYCYCLOPENTANE(931-94-2)

Safety Data

• Statements: 11
• Safety Statements: 9-16-33
• RIDADR: 3271
• HazardClass: 3
• PackingGroup: II
• Hazardous Substances Data: 931-94-2(Hazardous Substances Data)

Usage

Description

1,1-Dimethoxycyclopentane, with the molecular formula C7H14O2, is a cyclic ether that serves as a versatile solvent in a range of chemical reactions and processes. This colorless liquid, characterized by a boiling point of 126°C and a density of 0.94 g/mL, is known for its low reactivity and stability under normal conditions. Its low toxicity profile makes it a preferred choice for use in industrial and laboratory settings.

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

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

Downstream Products

• 1372122-76-3 C₂₀H₂₈O₄ 
• 67-56-1 methanol 
• 120-92-3 cyclopentanone 
• 161824-81-3 1-(2'-O,3'-O-Cyclopentyl-5'-hydroxy-β-D-erythro-pentofuranosyl)-N⁴-benzoylcytosine 
• 4884-13-3 1,1’-dihydroperoxydi(cyclopentyl)peroxide 
• 132606-28-1 1,1-bis(hydroperoxy)cyclopentane 
• 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 
• 112489-39-1 C₃₉H₄₂O₆ 
• 132089-82-8 6-(4-chlorophenylthio)-9-(2,3-O-cyclopentylidene-β-D-ribofuranosyl)-9H-purine 
• 106711-53-9 C₁₈H₂₄O₅ 
• 134311-79-8 C₁₈H₂₄O₅ 
• 112489-39-1 C₃₉H₄₂O₆ 
• 105065-63-2 (2S,3R)-2-(Benzyloxymethyl)-3-ethyl-1,4-dioxaspiro<4.4>nonane-2-carboxylic Acid 
• 105119-26-4 (2R,3R)-2-(Benzyloxymethyl)-3-ethyl-1,4-dioxaspiro<4.4>nonane-2-carboxylic Acid 

Relevant articles and documents

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.