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6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester is a versatile chemical compound widely utilized in organic synthesis and medicinal chemistry. It serves as a crucial building block for the development of pharmaceuticals and agrochemicals, owing to its boronic acid functionality that facilitates the formation of carbon-carbon bonds through Suzuki-Miyaura cross-coupling reactions. 6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester is also recognized for its potential as a ligand in metal-catalyzed reactions and as a key intermediate in the synthesis of biologically active molecules. The pinacol ester derivative enhances its stability and protects against side reactions, rendering it an invaluable asset in chemical synthesis.

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  • 485799-04-0 Structure
  • Basic information

    1. Product Name: 6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester
    2. Synonyms: 4-[5-(4,4,5,5-TETRAMETHYL-1,3,2-DIOXABOROLAN-2-YL)-2-PYRIDINYL]MORPHOLINE;4-[5-(4,4,5,5-TETRAMETHYL-[1,3,2]DIOXABOROLAN-2-YL)-PYRIDIN-2-YL]-MORPHOLINE;6-(MORPHOLIN-4-YL)PYRIDINE-3-BORONIC ACID PINACOL ESTER;6-MORPHOLINOPYRIDINE-3-BORONIC ACID, PINACOL ESTER;2-(4-MORPHOLINO)PYRIDINE-5-BORONIC ACID PINACOL ESTER;2-MORPHOLINOPYRIDINE-5-BORONIC ACID, PINACOL ESTER;2-(MORPHOLIN-4-YL)PYRIDINE-5-BORONIC ACID PINACOL ESTER;2-MORPHOLINE-4-YL-PYRIDINE-5-BORONIC ACID PINACOL ESTER
    3. CAS NO:485799-04-0
    4. Molecular Formula: C15H23BN2O3
    5. Molecular Weight: 290.17
    6. EINECS: N/A
    7. Product Categories: Amino;Organoborons;Pyridine;Boric Acid| Boric Acid Ester| Potassium Trifluoroborate
    8. Mol File: 485799-04-0.mol
  • Chemical Properties

    1. Melting Point: 135-139 °C(lit.)
    2. Boiling Point: 440.929 °C at 760 mmHg
    3. Flash Point: 220.466 °C
    4. Appearance: /
    5. Density: 1.13 g/cm3
    6. Vapor Pressure: 5.67E-08mmHg at 25°C
    7. Refractive Index: 1.53
    8. Storage Temp.: Keep in dark place,Sealed in dry,Room Temperature
    9. Solubility: N/A
    10. PKA: 5.58±0.10(Predicted)
    11. CAS DataBase Reference: 6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester(CAS DataBase Reference)
    12. NIST Chemistry Reference: 6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester(485799-04-0)
    13. EPA Substance Registry System: 6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester(485799-04-0)
  • Safety Data

    1. Hazard Codes: Xi,Xn
    2. Statements: 36/37/38-20/21/22
    3. Safety Statements: 22-24/25-45-43A-36/37/39-26
    4. RIDADR: 2811
    5. WGK Germany: 3
    6. RTECS:
    7. HazardClass: IRRITANT
    8. PackingGroup: N/A
    9. Hazardous Substances Data: 485799-04-0(Hazardous Substances Data)

485799-04-0 Usage

Uses

Used in Pharmaceutical Industry:
6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester is used as a key building block for the synthesis of various pharmaceuticals. Its boronic acid functionality allows for the formation of carbon-carbon bonds, enabling the creation of diverse drug molecules with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester is employed as a vital component in the development of agrochemicals. Its ability to form carbon-carbon bonds through cross-coupling reactions contributes to the synthesis of novel agrochemicals with improved efficacy and selectivity.
Used as a Ligand in Metal-Catalyzed Reactions:
6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester is utilized as a ligand in metal-catalyzed reactions. Its presence enhances the efficiency and selectivity of these reactions, leading to the production of desired products with fewer side reactions.
Used in the Synthesis of Biologically Active Molecules:
6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester is employed as a key intermediate in the synthesis of biologically active molecules. Its unique structure and reactivity enable the creation of molecules with potential applications in various biological and medicinal fields.
Used in Organic Synthesis:
6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester is used as a valuable tool in organic synthesis. Its pinacol ester derivative provides stability and protection against potential side reactions, making it an essential component in the synthesis of complex organic molecules.

Check Digit Verification of cas no

The CAS Registry Mumber 485799-04-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,8,5,7,9 and 9 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 485799-04:
(8*4)+(7*8)+(6*5)+(5*7)+(4*9)+(3*9)+(2*0)+(1*4)=220
220 % 10 = 0
So 485799-04-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H23BN2O3/c1-14(2)15(3,4)21-16(20-14)12-5-6-13(17-11-12)18-7-9-19-10-8-18/h5-6,11H,7-10H2,1-4H3

485799-04-0 Well-known Company Product Price

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  • (Code)Product description
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  • Alfa Aesar

  • (H50143)  6-(4-Morpholinyl)pyridine-3-boronic acid pinacol ester   

  • 485799-04-0

  • 250mg

  • 946.0CNY

  • Detail
  • Alfa Aesar

  • (H50143)  6-(4-Morpholinyl)pyridine-3-boronic acid pinacol ester   

  • 485799-04-0

  • 1g

  • 2879.0CNY

  • Detail
  • Aldrich

  • (654310)  6-(Morpholin-4-yl)pyridine-3-boronicacidpinacolester  97%

  • 485799-04-0

  • 654310-1G

  • 1,539.72CNY

  • Detail
  • Aldrich

  • (654310)  6-(Morpholin-4-yl)pyridine-3-boronicacidpinacolester  97%

  • 485799-04-0

  • 654310-5G

  • 5,583.24CNY

  • Detail

485799-04-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-(Morpholin-4-yl)pyridine-3-boronic acid pinacol ester

1.2 Other means of identification

Product number -
Other names 1-[5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-yl]morpholine

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:485799-04-0 SDS

485799-04-0Relevant articles and documents

INDOLE AHR INHIBITORS AND USES THEREOF

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, (2020/05/21)

The present invention provides compounds useful as inhibitors of AHR, compositions thereof, and methods of using the same.

1,4-BENZODIAZEPINONE COMPOUNDS AND THEIR USE IN TREATING CANCER

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Page/Page column 69, (2010/11/04)

The invention provides a family of 1,4-benzodiazepinone compounds and methods for their use as therapeutic agents in treating cancer. Pharmaceutical compositions and methods of making the 1,4-benzodiazepinone compounds are provided.

PHOSPHATIDYLINOSITOL 3 KINASE INHIBITORS

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Page/Page column 136, (2010/01/12)

Provided are compounds according to Formula (I), or stereoisomer, prodrug, polymorph, or pharmaceutically acceptable salt forms thereof, wherein X, Y, R1, R6 , R7, and R8 are as defined, which compounds are effective inhibitors of PI3-kinase and/or other medically and clinically relevant kinases. Also provided are pharmaceutical compositions and methods of using the compounds and compositions as PB -kinase and kinase inhibitors. More particularly, the compounds of the invention provide treatments and therapeutics for human diseases regulated by, or associated with, the activity of, PI3-kinases and/or protein kinases, or mutant or variant forms thereof.

KINASE INHIBITOR COMPOUNDS

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Page/Page column 41-42, (2008/12/07)

Pyridine and pyridazine derivatives have unexpected drug properties as inhibitors of protein kinases and are useful in treating disorders related to abnormal protein kinase activities such as cancer.

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