2041-15-8

Basic information

• Product Name: 1,3,5-Cyclohexanetriol
• Synonyms: Cyclohexane-1,3,5-triol;(1S,3S,5S)-CYCLOHEXANE-1,3,5-TRIOL;(1S,3S,5R)-CYCLOHEXANE-1,3,5-TRIOL;1,3,5-CYCLOHEXANETRIOL;phloroglucitol;1,3,5-CYCLOHEXANETRIOL (CIS+TRANS);1,3,5-CYCLOHEXANETRIOL (CIS- AND TRANS- MIXTURE);1,3,5-CYCLOHEXANETRIOL (CIS- AND TRANS- MIXTURE) 95+%
• CAS NO: 2041-15-8
• Molecular Formula: C₆H₁₂O₃
• Molecular Weight: 132.16
• Mol File: 2041-15-8.mol
• Article Data: 3

Chemical Properties

• Melting Point: 245 °C
• Boiling Point: 302.1 °C at 760 mmHg
• Flash Point: 154.2 °C
• Appearance: /
• Density: 1.356 g/cm³
• Vapor Pressure: 9.86E-05mmHg at 25°C
• Refractive Index: 1.58
• Storage Temp.: Sealed in dry,Room Temperature
• PKA: 14.22±0.60(Predicted)
• CAS DataBase Reference: 1,3,5-Cyclohexanetriol(CAS DataBase Reference)
• NIST Chemistry Reference: 1,3,5-Cyclohexanetriol(2041-15-8)
• EPA Substance Registry System: 1,3,5-Cyclohexanetriol(2041-15-8)

Safety Data

• Statements: 36/37/38
• Safety Statements: 26-36/37/39
• Hazardous Substances Data: 2041-15-8(Hazardous Substances Data)

Usage

General Description

1,3,5-Cyclohexanetriol is an organic compound, specifically a triol, with the chemical formula C6H12O3. This chemical is considered a polyol because it contains multiple hydroxy functional groups (-OH). As part of the cyclohexane family, this chemical features a six-membered ring structure. Its three hydroxyl groups are positioned at the 1, 3, and 5 points on the ring, giving it its name. It's mainly used in chemical or biochemical research, but specific details about its properties and effects are not widely documented, suggesting it's not commonly used in industrial applications or manufacturing processes.

InChI:InChI=1/C6H12O3/c7-4-1-5(8)3-6(9)2-4/h4-9H,1-3H2

Upstream product

• 108-73-6 3,5-dihydroxyphenol 
• 7732-18-5 water 
• 64-17-5 ethanol 
• 91-17-8 decalin 

Downstream Products

• 58890-26-9 1-phenyl-2,8,9-trioxa-1-sila-adamantane 
• 54049-24-0 methyl 7-bromoheptanoate 
• 88784-99-0 1-Brom-4-(2,4,10-trioxatricyclo<3.3.1.1^3,7>dec-3-yl)hexan 
• 6287-90-7 11-bromo-undecanoic acid methyl ester 
• 6271-23-4 11-bromoundecanoic acid ethyl ester 
• 88803-63-8 1-Brom-4-(2,4,10-trioxatricyclo<3.3.1.1^3,7>dec-3-yl)decan 
• 281-33-4 2,8,9-trioxa-1-phospha-adamantane 
• 187266-45-1 (3R,5S)-3,5-Bis-benzyloxy-cyclohexanone 
• 58006-28-3 trans-1,3,5-triacetoxy-cyclohexane 
• 327622-76-4 cis,cis-3,5-di(methylcarbonyloxy)cyclohexyl acetate 
• 187266-46-2 ((3S,5R)-3,5-Bis-benzyloxy-cyclohex-1-enyloxy)-trimethyl-silane 
• 875-12-7 α-Cyclohexantriol-(1a,3a,5a)-phosphat 
• 75543-69-0 Phenyl-(2,8,9-trioxa-1λ⁵-phospha-tricyclo[3.3.1.1^3,7]dec-1-ylidene)-amine 

Relevant articles and documents

Efficient and Practical Arene Hydrogenation by Heterogeneous Catalysts under Mild Conditions

An efficient and practical arene hydrogenation procedure based on the use of heterogeneous platinum group catalysts has been developed. Rh/C is the most effective catalyst for the hydrogenation of the aromatic ring, which can be conducted in iPrOH under neutral conditions and at ordinary to medium H 2 pressures (10 atm). A variety of arenes such as alkylbenzenes, benzoic acids, pyridines, furans, are hydrogenated to the corresponding cyclohexyl and heterocyclic compounds in good to excellet yields. The use of Ru/C, less expensive than Rh/C, affords an effective and practical method for the hydrogenation of arenes including phenols. Both catalysts can be reused several times after simple filtration without any significant loss of catalytic activity.

6-Substituted-4-hydroxy-tetrahydropyran-2-ones

6-Substituted-4-hydroxy-tetrahydropyran-2-ones, useful as anti-atherosclerotic agents, are obtainable by the process of the invention. The 6-substituents have a phenyl, naphthyl, tetrahydronaphthyl or indolyl nucleus bound through an ethenyl unit. The inv