41513-32-0

Basic information

• Product Name: TRANS-1,4-CYCLOHEXENEDIOL
• Synonyms: TRANS-1,4-CYCLOHEXENEDIOL;TRANS-2-CYCLOHEXENE-1,4-DIOL);trans-1,4-Cyclohexenediol,99%;trans-Cyclohex-2-ene-1,4-diol
• CAS NO: 41513-32-0
• Molecular Formula: C₆H₁₀O₂
• Molecular Weight: 114.14
• Mol File: 41513-32-0.mol
• Article Data: 12

Chemical Properties

• Melting Point: 84-87 °C
• Boiling Point: 173.66°C (rough estimate)
• Flash Point: 119.3°C
• Appearance: /
• Density: 1.0353 (rough estimate)
• Vapor Pressure: 0.00565mmHg at 25°C
• Refractive Index: 1.4495 (estimate)
• Storage Temp.: 0-6°C
• PKA: 14.14±0.40(Predicted)
• CAS DataBase Reference: TRANS-1,4-CYCLOHEXENEDIOL(CAS DataBase Reference)
• NIST Chemistry Reference: TRANS-1,4-CYCLOHEXENEDIOL(41513-32-0)
• EPA Substance Registry System: TRANS-1,4-CYCLOHEXENEDIOL(41513-32-0)

Safety Data

• Safety Statements: 24/25
• Hazardous Substances Data: 41513-32-0(Hazardous Substances Data)

Usage

Chemical Properties

WHITE TO SLIGHTLY BEIGE CRYSTALLINE POWDER

InChI:InChI=1/C6H10O2/c7-5-1-2-6(8)4-3-5/h1-2,5-8H,3-4H2/t5-,6-/m0/s1

Upstream product

• 1165952-91-9 cyclohexa-1,3-diene 
• 78776-44-0 trans-(±)-4-(acetoxy)cyclohex-2-en-1-yl acetate 
• 6705-51-7 3,4-epoxycyclohexene 
• 6705-51-7 1,3-cyclohexadiene monoepoxide 
• 20117-77-5 4-(acetoxy)cyclohex-2-en-1-yl acetate 
• 77300-22-2 benzoic acid 4-hydroxycyclohex-2-enyl ester 
• 108-93-0 cyclohexanol 

Downstream Products

• 6995-79-5 cyclohexane-1,4-diol 
• 132513-04-3 (+/-)-2ξ,3ξ-dibromo-cyclohexane-1r,4t-diol 
• 77300-23-3 trans-1,4-dibenzoyloxy-2-cyclohexene 
• 128014-56-2 9H-β-Carboline-3-carboxylic acid (1S,4S)-4-hydroxy-cyclohex-2-enyl ester 
• 73977-86-3 DL-trans-1,4-Di-O-benzylcyclohex-2-enediol 
• 76152-75-5 trans-4-methoxycyclohex-2-ene-1-ol 
• 59415-76-8 trans-1,4-dimethoxy-2-cyclohexene 
• 2975-92-0 d,l-(1,2,3/4)-cyclohexanetetrol 

Relevant articles and documents

Reductive Difunctionalization of Aryl Alkenes with Sodium Metal and Reduction-Resistant Alkoxy-Substituted Electrophiles

A general method for alkali-metal-promoted reductive difunctionalization of alkenes has been developed by means of reduction-resistant alkoxy-substituted electrophiles. A series of 1,2-diboration and 1,2-dicarbofunctionalization products can be synthesize

Expanding the scope of biomass-derived chemicals through tandem reactions based on oxorhenium-catalyzed deoxydehydration

New modes of DODH: Oxorhenium compounds act as deoxydehydration(DODH)/acid dual-purpose catalysts to transform biomass-derived diol substrates into a variety of commodity chemical precursors. The power of this approach is highlighted by a tandem [1,3]-OH shift/DODH of 2-ene-1,4-diols and 2,4-diene-1,6-diols, and by a DODH/esterification sequence of sugar acids to unsaturated esters for the production of polymers and plasticizers. Copyright

Metal-free borylative ring-opening of vinyl epoxides and aziridines

A rational approach towards the borylative ring-opening of vinylepoxides and vinylaziridines, by the in situ formed MeO-→bis(pinacolato) diboron adduct, has been developed. The enhanced nucleophilic character of the Bpin (sp2) moiety