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Tetrahydrofuran-3-boronic acid is a boronic acid derivative featuring a tetrahydrofuran ring attached to the boron atom, which serves as a versatile reagent in organic synthesis for the formation of carbon-carbon and carbon-heteroatom bonds.

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  • 260369-10-6 Structure
  • Basic information

    1. Product Name: TETRAHYDROFURAN-3-BORONIC ACID
    2. Synonyms: TETRAHYDROFURAN-3-BORONIC ACID;(Tetrahydrofuran-3-yl)boronic acid
    3. CAS NO:260369-10-6
    4. Molecular Formula: C4H9BO3
    5. Molecular Weight: 115.93
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 260369-10-6.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 268.2°C at 760 mmHg
    3. Flash Point: 116°C
    4. Appearance: /
    5. Density: 1.15g/cm3
    6. Vapor Pressure: 0.00105mmHg at 25°C
    7. Refractive Index: 1.446
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 10.16±0.20(Predicted)
    11. CAS DataBase Reference: TETRAHYDROFURAN-3-BORONIC ACID(CAS DataBase Reference)
    12. NIST Chemistry Reference: TETRAHYDROFURAN-3-BORONIC ACID(260369-10-6)
    13. EPA Substance Registry System: TETRAHYDROFURAN-3-BORONIC ACID(260369-10-6)
  • 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: 260369-10-6(Hazardous Substances Data)

260369-10-6 Usage

Uses

Used in Pharmaceutical Industry:
Tetrahydrofuran-3-boronic acid is used as a building block for the synthesis of complex organic molecules, particularly in the development of pharmaceuticals. Its unique structure and reactivity facilitate the formation of biaryl and heteroaryl compounds through Suzuki-Miyaura cross-couplings, which are crucial for the creation of novel drug candidates with improved therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, Tetrahydrofuran-3-boronic acid is employed as a key intermediate in the synthesis of agrochemicals. Its ability to form carbon-carbon and carbon-heteroatom bonds makes it an essential component in the development of new pesticides, herbicides, and other agrochemicals with enhanced efficacy and selectivity.
Used in Organic Synthesis:
Tetrahydrofuran-3-boronic acid is utilized as a versatile reagent in organic synthesis for the formation of various carbon-carbon and carbon-heteroatom bonds. Its unique structure and reactivity make it a valuable tool for the synthesis of complex organic molecules, including natural products, pharmaceuticals, and other specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 260369-10-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,0,3,6 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 260369-10:
(8*2)+(7*6)+(6*0)+(5*3)+(4*6)+(3*9)+(2*1)+(1*0)=126
126 % 10 = 6
So 260369-10-6 is a valid CAS Registry Number.
InChI:InChI=1/C4H9BO3/c6-5(7)4-1-2-8-3-4/h4,6-7H,1-3H2

260369-10-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name oxolan-3-ylboronic acid

1.2 Other means of identification

Product number -
Other names (Tetrahydrofuran-3-yl)boronic acid

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:260369-10-6 SDS

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