53067-09-7

Basic information

• Product Name: Cyclohexanepropanol, 2-hydroxy-
• Synonyms: 2-Hydroxy-1-(3-hydroxy-propyl)-cyclohexan;2-(3-Hydroxy-propyl)-cyclohexanol;Cyclohexanepropanol,2-hydroxy
• CAS NO: 53067-09-7
• Molecular Formula: C9H18O2
• Molecular Weight: 158.241
• Mol File: 53067-09-7.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: Cyclohexanepropanol, 2-hydroxy-(CAS DataBase Reference)
• NIST Chemistry Reference: Cyclohexanepropanol, 2-hydroxy-(53067-09-7)
• EPA Substance Registry System: Cyclohexanepropanol, 2-hydroxy-(53067-09-7)

Safety Data

• Hazardous Substances Data: 53067-09-7(Hazardous Substances Data)

Upstream product

• 4430-31-3 octahydrocoumarin 
• 2568-20-9 2-(3-oxopropyl)cyclohexanone 
• 1481-92-1 2-(3-hydroxypropyl)phenol 
• 82166-21-0 methyl cyclohexane 
• 4594-78-9 cyclohexanone-2-propionitrile 
• 10407-33-7 methyl 3-(2-oxocyclohexyl)propionate 
• 82726-01-0 3-(trans-2-hydroxycyclohexyl)propyl benzoate 
• 94088-21-8 trans-2-<2-(ethoxycarbonyl)ethyl>cyclohexanol 
• 4095-02-7 3-(2-oxocyclohexyl)propionic acid ethyl ester 
• 82726-01-0 Benzoic acid 3-((1R,2R)-2-hydroxy-cyclohexyl)-propyl ester 
• 60211-12-3 2-(3-hydroxypropyl)cyclohexan-1-ol 
• 24844-28-8 trans-2-allyl-1-cyclohexanol 

Downstream Products

• 22516-18-3 3-(cyclohex-1-en-1-yl)propan-1-ol 
• 344250-14-2 ((3-(cyclohex-1-en-1-yl)propoxy)methyl)benzene 
• 82725-83-5 3-(cyclohex-1-en-1-yl)propyl benzoate 
• 344268-52-6 C₁₆H₂₁⁽²⁾HO₂ 
• 82726-04-3 Benzoic acid 3-[(1R,2R)-2-(toluene-4-sulfonyloxy)-cyclohexyl]-propyl ester 
• 53067-09-7 trans-2-(3-hydroxypropyl)-cyclohexanol 
• 53067-09-7 cis-2-(3-hydroxypropyl)-cyclohexanol 
• 82725-85-7 trans-<2-(2)H>-2-(3-Hydroxypropyl)cyclohexanol 
• 82725-85-7 C₉H₁₇⁽²⁾HO₂ 
• 82725-84-6 trans-<2-(2)H>-2-(3-Benzyloxypropyl)cyclohexanol 
• 82725-84-6 cis-<2-(2)H>-2-(3-Benzyloxypropyl)cyclohexanol 
• 4430-31-3 trans-octahydro-1-benzopyran-2-one 
• 4430-31-3 octahydrocoumarin 
• 60211-17-8 3-((1R,2R)-2-Acetoxy-cyclohexyl)-propionic acid 3-((1S,2S)-2-acetoxy-cyclohexyl)-propyl ester 

Relevant articles and documents

PROCESS FOR PRODUCING HYDROXYMETHYL-ALCOHOLS

The present invention relates to a process for producing an organic compound A, which comprises at least one primary alcoholic hydroxy group and at least one secondary alcoholic hydroxy group, comprising a process step, wherein a compound B, which comprises at least one nitrile group and at least one ketone group, is reacted with hydrogen and water in the presence of at least one homogeneous transition metal catalyst TMC 1.

Bent bonds (τ) and the antiperiplanar hypothesis, and the reactivity at the anomeric center in pyranosides

The stereoselectivity of nucleophilic addition on oxocarbenium ions derived from the bicyclic pyranoside model with or without a C2-OR group can be understood through the use of the bent-bond and the antiperiplanar hypothesis in conjunction with the concept of hyperconjugation as an alternative interpretive model of structure and reactivity.

An unusual reaction of cyclic enol ethers with titanium(III) tetrahydroborate

Titanium(III) Tetrahydroborate formed in situ from titanium tetrachloride and benzyltriethylammonium tetrahydroborate (1:4) readily reacts with cyclic enol ethers in dichloromethane at -20°C to give the corresponding acyclic diols in high yields after simple aqueous work-up.