5763-53-1

Basic information

• Product Name: CYCLOPENTANE-1,1-DIYLDIMETHANOL
• Synonyms: CYCLOPENTANE-1,1-DIYLDIMETHANOL;1,1-Bis(hydroxymethyl)cyclopentane;1,1-Cyclopentanedimethanol;(1-methylolcyclopentyl)methanol;[1-(hydroxymethyl)cyclopentyl]methanol;NSC 49657
• CAS NO: 5763-53-1
• Molecular Formula: C₇H₁₄O₂
• Molecular Weight: 130.18486
• Mol File: 5763-53-1.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 257.7 °C at 760 mmHg
• Flash Point: 124.4 °C
• Appearance: /
• Density: 1.047 g/cm³
• Vapor Pressure: 0.00213mmHg at 25°C
• Refractive Index: 1.481
• CAS DataBase Reference: CYCLOPENTANE-1,1-DIYLDIMETHANOL(CAS DataBase Reference)
• NIST Chemistry Reference: CYCLOPENTANE-1,1-DIYLDIMETHANOL(5763-53-1)
• EPA Substance Registry System: CYCLOPENTANE-1,1-DIYLDIMETHANOL(5763-53-1)

Safety Data

• Hazardous Substances Data: 5763-53-1(Hazardous Substances Data)

Usage

General Description

CYCLOPENTANE-1,1-DIYLDIMETHANOL, also known as cyclopentanediol, is a chemical compound with the molecular formula C7H14O2. It is a colorless liquid with a mild, sweet odor and is commonly used as a solvent in various industrial applications. It is also utilized in the production of polyesters, polyurethanes, and other polymers. Additionally, it is employed in the synthesis of pharmaceuticals and agrochemicals. The compound is considered to have low toxicity and is not known to cause significant health hazards when handled and used appropriately. However, it should be handled with care and in accordance with proper safety protocols.

InChI:InChI=1/C7H14O2/c8-5-7(6-9)3-1-2-4-7/h8-9H,1-6H2

Upstream product

• 50-00-0 formaldehyd 
• 872-53-7 cyclopentanealdehyde 
• 4167-77-5 cyclopentane-1,1-dicarboxylic acid diethyl ester 
• 1449746-41-1 (cyclopentane-1,1-diylbis(methylene))bis(oxy)bis(tert-butyldimethylsilane) 
• 1449746-42-2 (cyclopentane-1,1-diylbis(methylene))bis(oxy)bis(triisopropylsilane) 
• 1449746-43-3 (cyclopentane-1,1-diylbis(methylene))bis(oxy)bis(tert-butyldiphenylsilane) 

Downstream Products

• 25451-50-7 1,1-Bis-carbamoyloxymethyl-cyclopentan 
• 68499-28-5 1,1-bis-(bromomethyl)-cyclopentane 
• 102539-92-4 1-hydroxymethyl-cyclopentanecarboxylic acid 
• 451472-23-4 2,3-diethyl(2R,3R)-1,4-dioxaspiro[4.4]nonane-2,3-dicarboxylate 
• 6140-63-2 1-methyl-1-cyclopentanecarbaldehyde 
• 583-60-8 2-Methylcyclohexanone 
• 2043-61-0 cyclohexanecarbaldehyde 
• 22308-10-7 Ditosylat des 1,1-bis(Hydroxymethyl)cyclopentans 
• 106280-86-8 1,1-Bis-hydroxymethyl-cyclopentan-bis-cyclohexylcarbamidsaeureester 
• 5779-54-4 Dicarbanilsaeureester des 1.1-Bis-hydroxymethyl-cyclopentans 
• 103423-51-4 1,1-Bis-hydroxymethyl-cyclopentan-bis-<4-carbethoxy-carbanilsaeureester> 
• 1192-37-6 methylenecyclohexane 
• 1276693-12-9 [1-(tert-butyl-dimethyl-silanyloxymethyl)-cyclopentyl]-methanol 
• 1276692-62-6 1-(1-(allyloxymethyl)cyclopentyl)-1-phenylprop-2-yn-1-ol 

Relevant articles and documents

GLYCOLATE OXIDASE INHIBITORS FOR THE TREATMENT OF DISEASE

Described herein are compounds, methods of making such compounds, pharmaceutical compositions and medicaments containing such compounds, and methods of using such compounds to treat or prevent diseases or disorders associated with a defect in glyoxylate metabolism, for example a disease or disorder associated with the enzyme glycolate oxidase (GO) or alterations in oxalate metabolism. Such diseases or disorders include, for example, disorders of glyoxylate metabolism, including primary hyperoxaluria, that are associated with production of excessive amounts of oxalate.

Helianthus-like cucurbit[4]uril and cucurbit[5]uril analogues

A new glycoluril-like molecule, cyclopentanopropanediurea (CyP-TD), was prepared by malonic ester synthesis. Its condensation with paraformaldehyde resulted in two Helianthus-like cucurbituril analogues, CyP4TD[4] and CyP5TD[5], with cyclopentano groups evenly distributed on the equators. The structures of the two macrocycles were confirmed by 1H-NMR, HRMS-ES and single-crystal X-ray diffraction. CyP4TD[4] and CyP5TD[5] both exhibit excellent thermal stability, and CyP5TD[5] has better solubility in water and organic solvents, while CyP4TD[4] can hardly dissolve in them.

Cerium(IV) sulfate tetrahydrate: A catalytic and highly chemoselective deprotection of THP, MOM, and BOM ethers

Tetrahydropyranyl (THP), methoxymethyl (MOM), and benzyloxymethyl (BOM) phenyl/alkyl ethers were efficiently cleaved to the corresponding parent hydroxyl compounds in good yields using catalytic amounts of Ce(SO 4)2·4H2O by microwave-assisted or conventional heating in methanol solution. Intramolecular and competitive experiments demonstrated the chemoselective deprotection of THP ethers in the presence of triisopropylsilyl (TIPS) and tert-butyldiphenylsilyl (TBDPS) phenyl ethers.