1088-01-3

Basic information

• Product Name: TRICYCLOHEXYL BORATE
• Synonyms: TRICYCLOHEXYL BORATE
• CAS NO: 1088-01-3
• Molecular Formula: C₁₈H₃₃B
• Molecular Weight: 308.26
• Mol File: 1088-01-3.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 362.3°C at 760 mmHg
• Flash Point: 172.9°C
• Appearance: /
• Density: 0.89g/cm³
• Vapor Pressure: 4.07E-05mmHg at 25°C
• Refractive Index: 1.477
• CAS DataBase Reference: TRICYCLOHEXYL BORATE(CAS DataBase Reference)
• NIST Chemistry Reference: TRICYCLOHEXYL BORATE(1088-01-3)
• EPA Substance Registry System: TRICYCLOHEXYL BORATE(1088-01-3)

Safety Data

• Hazardous Substances Data: 1088-01-3(Hazardous Substances Data)

Usage

General Description

Tricyclohexyl borate is a chemical compound commonly used as an additive in lubricants and hydraulic fluids to improve their thermal and oxidative stability. It is a boron-containing compound with a tricyclic structure, consisting of three cyclohexyl rings attached to a boron atom. Tricyclohexyl borate acts as a multifunctional additive, providing anti-wear, anti-oxidation, and anti-corrosion properties to lubricants and fluids. Its high thermal stability allows it to withstand high temperatures and prevent the formation of harmful deposits and sludge in the system. Overall, tricyclohexyl borate is a versatile additive that enhances the performance and longevity of lubricants and hydraulic fluids in a variety of industrial applications.

InChI:InChI=1/C18H33B/c1-4-10-16(11-5-1)19(17-12-6-2-7-13-17)18-14-8-3-9-15-18/h16-18H,1-15H2

Upstream product

• 1116-39-8 triisobutylborane 
• 110-82-7 cyclohexane 
• 931-50-0 cyclohexylmagnesium bromide 
• 110-83-8 cyclohexene 
• 111-96-6 diethylene glycol dimethyl ether 
• 109-99-9 tetrahydrofuran 
• 60-29-7 diethyl ether 
• 7446-70-0 aluminium trichloride 
• 19287-45-7 diborane 
• 110-51-0 borane pyridine 
• 7637-07-2 boron trifluoride 
• 1722-26-5 triethylamine-borane 
• 274-07-7 benzo[1,3,2]dioxaborole 
• 32999-09-0 2-cyclohexylbenzo-[d][1,3,2]dioxaborole 

Downstream Products

• 28289-86-3 cyclohexylboroxine 
• 98485-72-4 cyclo-C₆H₁₁BI₂ 
• 55382-85-9 B-iododicyclohexylborane 
• 66217-60-5 2-cyclohexyl-1,3,2-dioxaborolane 
• 67826-99-7 1,1-Dicyclohexyl-propan-1-ol 
• 27608-07-7 3-cyclohexylbutanal 
• 60217-91-6 Dicyclohexyl-(3-cyclohexyl-2-methyl-1-propenyloxy)-boran 
• 7122-93-2 3-cyclohexylcyclohexanone 
• 57476-24-1 dicyclohexyl(methylthio)borane 
• 26553-51-5 ethyl (3E)-4-cyclohexyl-3-butenoate 
• 42371-60-8 n-pentylcyclohexylacetylene 
• 67975-95-5 1-cyclohexyloct-1-ene 
• 52075-27-1 ethylsulfonyl-methylcyclohexane 
• 42716-73-4 ethyl 2-bromo-2-cyclohexylacetate 

Relevant articles and documents

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Divergence from the classical hydroboration reactivity; boron containing materials through a hydroboration cascade of small cyclic dienes

The hydroboration 1,3- and 1,4-cyclic dienes has been systematically investigated. The behavior of such dienes towards mono and dihydroboration was monitored directly by 11B NMR to identify the actual boron species formed, as opposed to the most common analysis of the resultant oxidation products. Quantitative dihydroboration was achieved for the full range of cyclic dienes investigated including dienes, which were previously reported to be resistant to dihydroboration, leading to the formation of new boron-containing polymeric materials. The conditions favoring dihydroboration are reported as well as full characterisation of the materials. Furthermore, a hydroboration cascade mechanism is proposed for the formation of such boron-containing polymers, supported by both experimental and theoretical data.

Generation of organolithium compounds bearing super silyl ester and their application to Matteson rearrangement

It's super-silyl-fragilithyl-ester-aryl-docious: The super silyl group is a strong protecting group for carboxylic acids and provides a method for direct lithiation that is compatible with the ester moiety. Organolithium compounds bearing a super silyl ester react with a variety of electrophiles in high yields (see scheme). The reaction of lithiated super silyl chloroacetate with a boron compound gives α-functionalization of the ester moiety by Matteson rearrangement. Copyright