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Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester is a chemical compound that belongs to the class of boronic acid esters. It features an imidazo[1,2-a]pyridine ring fused with a boronic acid group, offering unique properties that make it a valuable reagent in organic synthesis.

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  • 908268-52-0 Structure
  • Basic information

    1. Product Name: Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester
    2. Synonyms: Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester;IMidazo[1,2-a]pyridine,7-(4,4,5,5-tetraMethyl-1,3,2-dioxaborolan-2-yl)-;Imidazo[1,2-a]pyridin-7-ylboronic acid pinacol ester;7-(tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine;7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine
    3. CAS NO:908268-52-0
    4. Molecular Formula: C13H17BN2O2
    5. Molecular Weight: 244.1
    6. EINECS: N/A
    7. Product Categories: Organic boronic acid
    8. Mol File: 908268-52-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.12±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: under inert gas (nitrogen or Argon) at 2-8°C
    8. Solubility: N/A
    9. PKA: 6.50±0.50(Predicted)
    10. CAS DataBase Reference: Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester(CAS DataBase Reference)
    11. NIST Chemistry Reference: Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester(908268-52-0)
    12. EPA Substance Registry System: Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester(908268-52-0)
  • 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: 908268-52-0(Hazardous Substances Data)

908268-52-0 Usage

Uses

Used in Organic Synthesis:
Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester is used as a reagent in various chemical reactions, such as Suzuki-Miyaura cross-coupling reactions, for the introduction of the imidazo[1,2-a]pyridine moiety into organic or pharmaceutical compounds. Its stability and easy handling make it a preferred choice in organic synthesis.
Used in Pharmaceutical Development:
Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester is utilized in the development of new pharmaceuticals due to the unique properties of the imidazo[1,2-a]pyridine ring. Its potential applications in drug discovery are being explored for the creation of novel therapeutic agents.
Used in Agrochemical Development:
Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester is also used in the development of new agrochemicals, where the imidazo[1,2-a]pyridine ring may contribute to the design of effective and targeted pesticides or other agricultural products.
Used in Material Science:
Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester has the potential to be utilized in the development of new materials, capitalizing on the structural and functional attributes of the imidazo[1,2-a]pyridine system to create innovative materials with specific properties.
Further research and exploration of Imidazo[1,2-a]pyridine-7-boronic acid pinacol ester's potential applications are ongoing across these industries, indicating its broad utility and the possibility of future discoveries in its application space.

Check Digit Verification of cas no

The CAS Registry Mumber 908268-52-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,8,2,6 and 8 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 908268-52:
(8*9)+(7*0)+(6*8)+(5*2)+(4*6)+(3*8)+(2*5)+(1*2)=190
190 % 10 = 0
So 908268-52-0 is a valid CAS Registry Number.

908268-52-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)imidazo[1,2-a]pyridine

1.2 Other means of identification

Product number -
Other names 7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)H-imidazo[1,2-a]pyridine

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:908268-52-0 SDS

908268-52-0Relevant articles and documents

Transition metal complex, polymer, mixture, composition and organic electronic device

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Paragraph 0419; 0423-0425, (2020/05/01)

The invention discloses a transition metal complex, a polymer, a mixture, a composition and an organic electronic device. The transition metal complex has a structural general formula represented by achemical formula (1), and is simple to synthesize, novel in structure, relatively good in stability, long in service life and good in light emitting performance; the compound represented by the chemical formula (1) is convenient for realizing an efficient, high-brightness and high-stability OLED device, and a relatively good material option is provided for full-color display and illumination application.

IMIDAZO [1,5-A]PYRIMIDINYL CARBOXAMIDE COMPOUNDS AND THEIR USE IN THE TREATMENT OF MEDICAL DISORDERS

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Paragraph 00516, (2017/11/04)

The invention provides substituted imidazo[1,5-a]pyrimidinyl carboxamide and related organic compounds, compositions containing such compounds, medical kits, and methods for using such compounds and compositions to treat medical disorders, e.g., Gaucher disease, Parkinson's disease, Lewy body disease, dementia, or multiple system atrophy, in a patient. Exemplary substituted imidazo[1,5-a]pyrimidinyl carboxamide compounds described herein include substituted 2-heterocyclyl-4-alkyl-imidazo[1,5-a]pyrirnidine-8-carboxamide compounds and variants thereof.

Imidazo [1,2-a] pyridine-6-boronic acid frequency ester and its derivatives preparation method

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Paragraph 0059-0064, (2016/10/17)

The invention discloses preparation methods for imidazole[1,2-a]pyridine-6-boric acid pinacol ester and derivatives thereof. The preparation methods comprise a preparation method for imidazole[1,2-a]pyridine-6-boric acid pinacol ester, a preparation method for imidazole[1,2-a]pyridine-7-boric acid pinacol ester and a preparation method for imidazole[1,2-a]pyridine-8-boric acid pinacol ester. The imidazole[1,2-a]pyridine-6-boric acid pinacol ester and derivatives thereof prepared by using the preparation methods are used in the Suzuki coupling reaction for a coupling reaction with compounds like halides and TfO-R. According to a technical scheme in the invention, the preparation methods have the advantages of high reaction yield, easy purification, suitability for production, etc.

FATTY ACID SYNTHASE INHIBITORS

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Page/Page column 58-59, (2014/01/18)

This invention relates to novel spirocyclic piperidines according to Formula (I) which are inhibitors of fatty acid synthase (FAS), to pharmaceutical compositions containing them, to processes for their preparation, and to their use in therapy for the treatment of cancers.

IMIDAZO [1,2-A]PYRIDINE DERIVATIVES AS FGFR KINASE INHIBITORS FOR USE IN THERAPY

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Page/Page column 36, (2012/03/08)

The invention relates to new bicyclic heterocyclyl derivatives of formula (I), to pharmaceutical compositions comprising said compounds and to the use of said compounds in the treatment of diseases, e.g. cancer.

IMIDAZOPYRIDINE DERIVATIVES AS INHIBITORS OF RECEPTOR TYROSINE KINASES

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, (2010/01/07)

The invention relates to new bicyclic heterocyclic derivative compounds, to pharmaceutical compositions comprising said compounds and to the use of said compounds in the treatment of diseases, e.g. cancer.

CYCLOHEXYLPYRAZOLE-LACTAM DERIVATIVES AS INHIBITORS OF 11-BETA-HYDROXYSTEROID DEHYDROGENASE 1

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Page/Page column 45, (2009/05/29)

The present invention discloses novel compounds of Formula (I): having 11β-HSD type 1 antagonist activity, as well as methods for preparing such compounds. In another embodiment, the invention discloses pharmaceutical compositions comprising compound

IMIDAZO (1, 2-A) PYRIDINE COMPOUNDS AS VEGF-R2 INHIBITORS

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Page/Page column 27, (2008/06/13)

The present invention provides compounds that are inhibitors of VEGF-R2 of the formula: (I) and methods of using these compounds.

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