50409-12-6

Basic information

• Product Name: CIS,CIS-1,3,5-CYCLOHEXANETRIOL DIHYDRATE
• Synonyms: CIS-1,3,5-TRIHYDROXYCYCLOHEXANE;CIS,CIS-1,3,5-CYCLOHEXANETRIOL DIHYDRATE;CIS,CIS-1,3,5-TRIHYDROXYCYCLOHEXANE DIHYDRATE;CIS-PHLOROGLUCITOL DIHYDRATE;1,3,5-Cyclohexanetriol, (1.alpha.,3.alpha.,5.alpha.)-;(1alpha,3alpha,5alpha)-1,3,5-Cyclohexanetriol;-cyclohexane-1,3,5-triol dihydrate;(1α,3α,5α)-1,3,5-Cyclohexanetriol
• CAS NO: 50409-12-6
• Molecular Formula: C₆H₁₂O₃
• Molecular Weight: 132.16
• Mol File: 50409-12-6.mol
• Article Data: 4

Chemical Properties

• Melting Point: 108-111 °C(lit.)
• Boiling Point: 492.4 °C at 760 mmHg
• Flash Point: 251.6 °C
• Appearance: /
• Density: 1.356g/cm³
• Vapor Pressure: 9.86E-05mmHg at 25°C
• Refractive Index: 1.58
• Solubility: soluble in Methanol
• PKA: 14.22±0.60(Predicted)
• CAS DataBase Reference: CIS,CIS-1,3,5-CYCLOHEXANETRIOL DIHYDRATE(CAS DataBase Reference)
• NIST Chemistry Reference: CIS,CIS-1,3,5-CYCLOHEXANETRIOL DIHYDRATE(50409-12-6)
• EPA Substance Registry System: CIS,CIS-1,3,5-CYCLOHEXANETRIOL DIHYDRATE(50409-12-6)

Safety Data

• WGK Germany: 3
• Hazardous Substances Data: 50409-12-6(Hazardous Substances Data)

Usage

Uses

cis,cis-1,3,5-Cyclohexanetriol Dihydrate is a hydrogenated derivative of Phloroglucinol (P340000); an antispasmodic.

InChI:InChI=1/C6H12O3/c7-4-1-5(8)3-6(9)2-4/h4-9H,1-3H2/t4-,5+,6-

Upstream product

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

Downstream Products

• 157371-80-7 3-(bromomethyl)-2,4,10-trioxaadamantane 
• 281-33-4 2,8,9-trioxa-1-phospha-adamantane 
• 875-12-7 2,8,9-trioxa-1-phospha-adamantane-1-oxide 
• 64747-25-7 cis,cis-1,3,5-cyclohexanetritosylate 
• 74091-54-6 3-Phenyl-2,4,10-trioxa-adamantane 
• 31044-88-9 cis-1,3,5-Tris(phenylsulfonyloxy)cyclohexane 
• 140706-58-7 all-cis-3-(3,5-di(3-carboxypropanoyloxy)cyclohexoxycarbonyl)propanoic acid 
• 91362-54-8 3-(4-chlorophenyl)-2,4,10-trioxaadamantane 
• 91362-56-0 3-(4-nitrophenyl)-2,4,10-trioxaadamantane 
• 91362-53-7 3-(4-methylphenyl)-2,4,10-trioxaadamantane 
• 91362-62-8 3-(2,4-dimethylphenyl)-2,4,10-trioxaadamantane 
• 92808-55-4 1-(1-Phenyl-ethyl)-2,8,9-trioxa-1-sila-tricyclo[3.3.1.1^3,7]decane 
• 92808-52-1 Dimethyl-[4-(2,8,9-trioxa-1-sila-tricyclo[3.3.1.1^3,7]dec-1-yl)-phenyl]-amine 
• 92808-57-6 1-Cyclohexyl-2,8,9-trioxa-1-sila-tricyclo[3.3.1.1^3,7]decane 

Relevant articles and documents

Concise total synthesis of AB5046A and AB5046B

Two naturally occurring rare 5-oxo β-triketones, AB5046A and AB5046B, were efficiently synthesized in five linear steps with overall yields of 36% and 28%, respectively. The synthetic strategy highlighted the readily preparation of the key intermediate, 3

Compounds with Urotropine Structure, LX. - Orthooxalic and Orthocarbonic Acid Derivatives with Adamantane Structure

Methyl trimethoxyacetate (1) and cis-1,3,5-cyclohexanetriol (2) easily react to give methyl 2,4,10-trioxaadamantane-3-carboxylate (3).Based on 3, further derivates of 2,4,10-trioxaadamantane are prepared.By degradation reactions, 3-bromo- and 3-amino-2,4,