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1H-Indazole, 6-bromo-3-fluoro-4-nitro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1198437-02-3 Structure
  • Basic information

    1. Product Name: 1H-Indazole, 6-bromo-3-fluoro-4-nitro-
    2. Synonyms:
    3. CAS NO:1198437-02-3
    4. Molecular Formula:
    5. Molecular Weight: 260.022
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1198437-02-3.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: 1H-Indazole, 6-bromo-3-fluoro-4-nitro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1H-Indazole, 6-bromo-3-fluoro-4-nitro-(1198437-02-3)
    11. EPA Substance Registry System: 1H-Indazole, 6-bromo-3-fluoro-4-nitro-(1198437-02-3)
  • 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: 1198437-02-3(Hazardous Substances Data)

1198437-02-3 Usage

Heterocyclic aromatic compound

A compound containing a fused dihydroindole ring system This property means that 1H-Indazole, 6-bromo-3-fluoro-4-nitrohas a ring structure containing both carbon and nitrogen atoms, which contributes to its stability and aromatic character.

Fused dihydroindole ring system

A structural feature of the compound The presence of this ring system gives the compound a specific three-dimensional shape and may influence its reactivity and interactions with other molecules.

Bromine atom

A halogen atom attached to the indazole ring The bromine atom provides the compound with additional reactivity and may be involved in substitution or elimination reactions.

Fluorine atom

A halogen atom attached to the indazole ring The presence of the fluorine atom can influence the compound's electronic properties and may be involved in various chemical reactions.

Nitro group

A -NO2 functional group attached to the indazole ring The nitro group is a strong electron-withdrawing group that can affect the reactivity of the compound and may be involved in reduction or other chemical reactions.

Building block in synthesis

Used in the synthesis of other organic compounds Due to its unique structure and reactivity, 1H-Indazole, 6-bromo-3-fluoro-4-nitrocan be used as a starting material or intermediate in the synthesis of more complex organic compounds.

Potential applications in pharmaceutical and material science research

Possible uses in drug development and material design The compound's unique properties and reactivity may make it a valuable component in the development of new drugs or materials with specific functions or characteristics.

Check Digit Verification of cas no

The CAS Registry Mumber 1198437-02-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,8,4,3 and 7 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1198437-02:
(9*1)+(8*1)+(7*9)+(6*8)+(5*4)+(4*3)+(3*7)+(2*0)+(1*2)=183
183 % 10 = 3
So 1198437-02-3 is a valid CAS Registry Number.

1198437-02-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-bromo-3-fluoro-4-nitro-1H-indazole

1.2 Other means of identification

Product number -
Other names -

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:1198437-02-3 SDS

1198437-02-3Upstream product

1198437-02-3Relevant articles and documents

BROMODOMAIN INHIBITOR

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Paragraph 0364, (2016/10/31)

The present invention relates to substituted heterocyclic derivative compounds, compositions comprising said compounds, and the use of said compounds and compositions for epigenetic regulation by inhibition of bromodomain-mediated recognition of acetyl lysine regions of proteins, such as histones. Said compositions and methods are useful for the treatment of cancer and neoplastic disease.

Indazole derivatives for use in the treatment of influenza virus infection

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Page/Page column 140; 141, (2016/06/01)

The present invention is directed to compounds for use in the treatment or prevention of influenza virus infection.

NOVEL COMPOUNDS

-

Page/Page column 69-70, (2011/06/25)

The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I): and salts thereof. The compounds of the invention are inhibitors of PI3-kinase activity.

BENZPYRAZOLE DERIVATIVES AS INHIBITORS OF P13 KINASES

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Page/Page column 76, (2011/06/25)

The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of PI3-kinase activity.

NOVEL COMPOUNDS

-

Page/Page column 81-82, (2009/12/28)

The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of PI3-kinase activity.

BENZPYRAZOL DERIVATIVES AS INHIBITORS OF PI3 KINASES

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Page/Page column 137-138, (2009/12/28)

The invention is directed to certain novel compounds. Specifically, the invention is directed to compounds of formula (I) and salts thereof. The compounds of the invention are inhibitors of PI3-kinase activity.

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