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932382-18-8

N,N-diethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide is a complex organic compound characterized by its multiple functional groups, including a picolinamide moiety and a dioxaborolane group. This molecule is known for its strong chelating ability due to the picolinamide group, which allows it to form stable complexes with metal ions. The dioxaborolane group contributes to the molecule's versatility, enabling it to engage in a range of chemical reactions, such as the Suzuki-Miyaura cross-coupling. Its unique properties and reactivity make it an essential component in the development of new materials, pharmaceuticals, and agrochemicals.

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  • N,N-Diethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-Pyridinecarboxamide

    Cas No: 932382-18-8

  • USD $ 1.9-2.9 / Gram

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  • 932382-18-8 Structure

  • Basic information

    1. Product Name: N,N-DIETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PICOLINAMIDE
    2. Synonyms: N,N-DIETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PICOLINAMIDE;N,N-Diethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-Pyridinecarboxamide;N,N-diethyl-4-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)nicotinaMide
    3. CAS NO:932382-18-8
    4. Molecular Formula: C16H25BN2O3
    5. Molecular Weight: 304.19
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 932382-18-8.mol

  • Chemical Properties

    1. Melting Point: 130-135 °C (sublm)(Solv: hexane (110-54-3); dichloromethane (75-09-2))
    2. Boiling Point: 453.4°C at 760 mmHg
    3. Flash Point: 228°C
    4. Appearance: /
    5. Density: 1.07g/cm3
    6. Vapor Pressure: 2.07E-08mmHg at 25°C
    7. Refractive Index: 1.509
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 3.17±0.20(Predicted)
    11. CAS DataBase Reference: N,N-DIETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PICOLINAMIDE(CAS DataBase Reference)
    12. NIST Chemistry Reference: N,N-DIETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PICOLINAMIDE(932382-18-8)
    13. EPA Substance Registry System: N,N-DIETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PICOLINAMIDE(932382-18-8)

  • 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: 932382-18-8(Hazardous Substances Data)

932382-18-8 Usage

Uses

Used in Coordination Chemistry:
N,N-diethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide is used as a ligand for its strong chelating ability, which enables the formation of stable complexes with metal ions. This application is crucial in coordination chemistry for studying metal ion interactions and developing new coordination compounds.
Used in Organic Synthesis:
In the field of organic synthesis, N,N-diethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide serves as a valuable precursor. Its dioxaborolane group allows it to participate in various chemical reactions, such as the Suzuki-Miyaura cross-coupling, which is widely used for the formation of carbon-carbon bonds in the synthesis of complex organic molecules.
Used in the Development of New Materials:
The unique properties and reactivity of N,N-diethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide make it an essential component in the development of new materials. Its ability to form stable complexes with metal ions and participate in various chemical reactions contributes to the creation of materials with novel properties and potential applications.
Used in Pharmaceutical and Agrochemical Industries:
Due to its strong chelating ability and versatility in chemical reactions, N,N-diethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)picolinamide plays a crucial role in the development of new pharmaceuticals and agrochemicals. It can be used as a building block or a modifying agent in the synthesis of bioactive compounds, potentially leading to the discovery of new drugs and agrochemicals with improved efficacy and selectivity.

Check Digit Verification of cas no

The CAS Registry Mumber 932382-18-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,2,3,8 and 2 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 932382-18:
(8*9)+(7*3)+(6*2)+(5*3)+(4*8)+(3*2)+(2*1)+(1*8)=168
168 % 10 = 8
So 932382-18-8 is a valid CAS Registry Number.
InChI:InChI=1/C16H25BN2O3/c1-7-19(8-2)14(20)12-11-18-10-9-13(12)17-21-15(3,4)16(5,6)22-17/h9-11H,7-8H2,1-6H3

932382-18-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N-Diethyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-3-Pyridinecarboxamide

1.2 Other means of identification

Product number -
Other names N,N-DIETHYL-4-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)PICOLINAMIDE

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:932382-18-8 SDS

932382-18-8Downstream Products

932382-18-8Relevant articles and documents

Directed ortho metalation-boronation and Suzuki-Miyaura cross coupling of pyridine derivatives: A one-pot protocol to substituted azabiaryls

Alessi, Manlio,Larkin, Andrew L.,Ogilvie, Kevin A.,Green, Laine A.,Lai, Sunny,Lopez, Simon,Snieckus, Victor

, p. 1588 - 1594 (2008/02/03)

A general method for the synthesis of azabiaryls 19a-t by a one-pot procedure involving a Directed ortho metalation (DoM)-boronation-Suzuki-Miyaura cross coupling sequence is described. Aside from the three isomeric pyridyl carboxamides 15a-c, chloro-, fl

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