14983-42-7

Basic information

• Product Name: tris(2-methoxyethyl) orthoborate
• Synonyms: tris(2-methoxyethyl) orthoborate;tris(2-methoxyethyl) borate;Boric acid tris(2-methoxyethyl) ester;Tris(2-methoxyethoxy) boron;Tris(2-methoxyethoxy)borane;Einecs 239-064-1;Ethanol, 2-methoxy-, 1,1',1''-triester with boric acid (H3bo3);Ethanol, 2-methoxy-, triester with boric acid (H3bo3)
• CAS NO: 14983-42-7
• Molecular Formula: C₉H₂₁BO₆
• Molecular Weight: 236.07044
• EINECS: 239-064-1
• Mol File: 14983-42-7.mol
• Article Data: 7

Chemical Properties

• Boiling Point: 263 °C at 760 mmHg
• Flash Point: 99.1 °C
• Appearance: /
• Density: 0.995 g/cm³
• Vapor Pressure: 0.0173mmHg at 25°C
• Refractive Index: 1.401
• Storage Temp.: Hygroscopic, Refrigerator, under inert atmosphere
• Solubility: Benzene (Slightly), Chloroform (Slightly), Methanol (Slightly, Heated)
• Stability: Moisture Sensitive
• CAS DataBase Reference: tris(2-methoxyethyl) orthoborate(CAS DataBase Reference)
• NIST Chemistry Reference: tris(2-methoxyethyl) orthoborate(14983-42-7)
• EPA Substance Registry System: tris(2-methoxyethyl) orthoborate(14983-42-7)

Safety Data

• Hazardous Substances Data: 14983-42-7(Hazardous Substances Data)

Usage

Uses

Tris(2-methoxyethyl)orthoborate (>90%) can be used to produce a dynamic polymer with hybrid crosslinked structure for damping and cushioning materials, impact-?resistant protective materials, shape memory materials, self-?repairing materials and tough materials.

InChI:InChI=1/C9H21BO6/c1-11-4-7-14-10(15-8-5-12-2)16-9-6-13-3/h4-9H2,1-3H3

Upstream product

• 109-86-4 2-methoxy-ethanol 
• 11113-50-1 boric acid 

Downstream Products

• 163759-49-7 2'-O-(2-methoxyethyl)-5-methyluridine 
• 65-71-4 thymin 
• 163759-50-0 5'-O-(4,4'-dimethoxytriphenylmethyl)-2'-O-(2-methoxyethyl)-5-methyluridine 
• 143-66-8 sodium tetraphenyl borate 

Relevant articles and documents

FT-IR and NMR study of tris(oxaalkyl) borates and their complexes with HAuCl4

Three tris(oxaalkyl) borates and their complexes with HAuCl4 were studied by FT-IR, 1H and 13C NMR spectroscopy. Continuous absorption in the FT-IR spectra of the complexes testifies the formation of proton channels showing large proton polarizability. The shape of the proton potential is discussed on the basis of the NM -data. (C) 2000 Elsevier Science B.V.

Multinuclear NMR studies of tris(oxaalkyl) borates and their complexes with some metal cations

Nuclear magnetic resonance (NMR) of 1H, 13C, 11B and 17O nuclei has been used for the study of complexation of CoCl2, NiCl2 and CuCl2 salts with three tris(oxaalkyl) borates. All NMR techniques demonstrated the formation of complexes but the most informative were the 13C and 17O NMR measurements. The structures of the complexes formed are discussed in this article.

TRICYANOBORATE ALKYL ETHERS

The invention relates to tricyanoborate alkyl ethers, a method for their preparation and their use as ionic liquids.