Welcome to LookChem.com Sign In|Join Free

CAS

  • or

7359-98-0

2,4,6-Tributylboroxin, with the molecular formula C15H33BO3, is a boron-based chemical compound that serves as a versatile catalyst in organic synthesis. It is recognized for its capacity to expedite a range of chemical reactions, particularly in the formation of carbon-carbon bonds and the transformation of organic compounds. This colorless, odorless liquid is characterized by a low melting and boiling point, facilitating its ease of handling and storage in laboratory conditions. Its applications extend beyond catalysis, with potential in medicinal chemistry and materials science.

7359-98-0 Suppliers

Post Buying Request

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier
  • 7359-98-0 Structure

  • Basic information

    1. Product Name: 2,4,6-Tributylboroxin
    2. Synonyms: 2,4,6-Tributylboroxin;Tributylboroxin
    3. CAS NO:7359-98-0
    4. Molecular Formula: C12H27B3O3
    5. Molecular Weight: 251.774
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 7359-98-0.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 271.2°Cat760mmHg
    3. Flash Point: 117.8°C
    4. Appearance: /
    5. Density: 0.86g/cm3
    6. Vapor Pressure: 0.0109mmHg at 25°C
    7. Refractive Index: 1.401
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 2,4,6-Tributylboroxin(CAS DataBase Reference)
    11. NIST Chemistry Reference: 2,4,6-Tributylboroxin(7359-98-0)
    12. EPA Substance Registry System: 2,4,6-Tributylboroxin(7359-98-0)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 7359-98-0(Hazardous Substances Data)

7359-98-0 Usage

Uses

Used in Organic Synthesis:
2,4,6-Tributylboroxin is used as a catalyst for facilitating various organic reactions, primarily due to its ability to enhance the formation of carbon-carbon bonds and the conversion of organic compounds into different forms. Its efficiency in these processes makes it a valuable tool in the synthesis of complex organic molecules.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 2,4,6-Tributylboroxin is utilized as a reagent in the development of pharmaceutical compounds. Its unique catalytic properties allow for the synthesis of novel drug candidates, potentially leading to the discovery of new therapeutic agents.
Used in Materials Science:
2,4,6-Tributylboroxin also finds application in materials science, where it is employed in the synthesis of advanced materials with specific properties. Its role in creating new materials can contribute to the development of innovative products in various industries.
The provided materials do not specify different industries for the applications of 2,4,6-Tributylboroxin, hence the uses are generalized across the fields of organic synthesis, medicinal chemistry, and materials science.

Check Digit Verification of cas no

The CAS Registry Mumber 7359-98-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,5 and 9 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7359-98:
(6*7)+(5*3)+(4*5)+(3*9)+(2*9)+(1*8)=130
130 % 10 = 0
So 7359-98-0 is a valid CAS Registry Number.
InChI:InChI=1/C12H27B3O3/c1-4-7-10-13-16-14(11-8-5-2)18-15(17-13)12-9-6-3/h4-12H2,1-3H3

7359-98-0SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,4,6-tributyl-1,3,5,2,4,6-trioxatriborinane

1.2 Other means of identification

Product number -
Other names n-butyl boroxol

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7359-98-0 SDS

7359-98-0Relevant articles and documents

Low-Temperature Hypergolic Ignition of 1-Octene with Low Ignition Delay Time

Sheng, Haoqiang,Huang, Xiaobin,Chen, Zhijia,Zhao, Zhengchuang,Liu, Hong

, p. 423 - 434 (2021/02/05)

The attainment of the efficient ignition of traditional liquid hydrocarbons of scramjet combustors at low flight Mach numbers is a challenging task. In this study, a novel chemical strategy to improve the reliable ignition and efficient combustion of hydrocarbon fuels was proposed. A directional hydroboration reaction was used to convert hydrocarbon fuel into highly active alkylborane, thereby leading to changes in the combustion reaction pathway of hydrocarbon fuel. A directional reaction to achieve the hypergolic ignition of 1-octene was designed and developed by using Gaussian simulation. Borane dimethyl sulfide (BDMS), a high-energy additive, was allowed to react spontaneously with 1-octene to achieve the hypergolic ignition of liquid hydrocarbon fuel at -15 °C. Compared with the ignition delay time of pure 1-octene (565 °C), the ignition delay time of 1-octene/BDMS (9:1.2) decreased by 3850% at 50 °C. Fourier transform infrared spectroscopy and gas chromatography-mass spectrometry confirmed the directional reaction of the hypergolic ignition reaction pathway of 1-octene and BDMS. Moreover, optical measurements showed the development trend of hydroxyl radicals (OH·) in the lower temperature hypergolic ignition and combustion of 1-octene. Finally, this study indicates that the enhancement of the low-temperature ignition performance of 1-octene by hydroboration in the presence of BDMS is feasible and promising for jet propellant design with tremendous future applications.

Study of the radical chemistry promoted by tributylborane

Liu, Shujuan,Zheng, Zhen,Li, Minrui,Wang, Xinling

, p. 1893 - 1907 (2013/02/23)

The structures of radicals generated in the oxidation process of trialkylborane were detected based on ultra-high performance liquid chromatographyquadrupole-time-of-flight mass spectrometry (UPLC/Q-ToF MS) combined with the spin trapping method. Structur

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 7359-98-0