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CAS

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1973485-26-5

N-(5-bromoimidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1973485-26-5 Structure

  • Basic information

    1. Product Name: N-(5-bromoimidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide
    2. Synonyms:
    3. CAS NO:1973485-26-5
    4. Molecular Formula:
    5. Molecular Weight: 280.124
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1973485-26-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: N-(5-bromoimidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-(5-bromoimidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide(1973485-26-5)
    11. EPA Substance Registry System: N-(5-bromoimidazo[1,2-a]pyridin-2-yl)cyclopropanecarboxamide(1973485-26-5)

  • 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: 1973485-26-5(Hazardous Substances Data)

1973485-26-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1973485-26-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,9,7,3,4,8 and 5 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1973485-26:
(9*1)+(8*9)+(7*7)+(6*3)+(5*4)+(4*8)+(3*5)+(2*2)+(1*6)=225
225 % 10 = 5
So 1973485-26-5 is a valid CAS Registry Number.

1973485-26-5Downstream Products

1973485-26-5Relevant articles and documents

METHOD FOR PREPARING SUBSTITUTED IMIDAZO[1,2-A]PYRIDIN-2-YLAMIDE COMPOUND, AND INTERMEDIATE THEREOF

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, (2022/02/24)

A method for preparing a substituted imidazo[1,2-a]pyridin-2-ylamide compound and an intermediate thereof. Specifically disclosed is a method for preparing a compound represented by formula I: R1 is C1-C6 alkyl or C3-C8 cycloalkyl; R2 and R3 are independently selected from halogen and C1-C6 alkyl; R4 is Br, I or OTf, preferably being Br; and m and n are each independently 0, 1, 2, 3, or 4. The preparation method for synthesizing the compound represented by formula I features simple operation, easy control of product quality, and a high yield and is suitable for industrial production.

SALT FORM AND CRYSTAL FORM OF JAK INHIBITOR, PREPARATION METHOD THEREFOR, AND USE THEREOF

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, (2022/02/24)

Provided in the present invention are a salt form and a crystal form of a JAK inhibitor, a preparation method therefor, and the use thereof. An X-ray powder diffraction pattern of a crystal form A of a compound as shown in formula I has characteristic diffraction peaks at the 2θ angles of 5.9°±0.2°, 7.4°±0.2°, 11.6°±0.2°, 21.7°±0.2° and 23.8°±0.2°.

SUBSTITUTED IMIDAZO [1, 2-A] PYRIDIN-2-YLAMINE COMPOUNDS, AND PHARMACEUTICAL COMPOSITIONS AND METHODS OF USE THEREOF

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, (2016/08/23)

Provided herein are substituted imidazo [1, 2-a] pyridin-2-ylamine compounds, for example, of formula (A), and pharmaceutical compositions thereof; and methods of their use for treating, preventing, or ameliorating one or more symptoms of a Janus kinase-m

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