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CAS

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383137-41-5

1-(2-bromo-4-fluorophenyl)-1H-pyrrole is a chemical compound belonging to the pyrrole family, characterized by a five-membered heterocyclic ring with a nitrogen atom. It has the molecular formula C10H7BrFN and is recognized for its potential applications in the pharmaceutical and agrochemical industries, as well as its antimicrobial and antifungal properties.

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  • 383137-41-5 Structure

  • Basic information

    1. Product Name: 1-(2-bromo-4-fluorophenyl)-1H-pyrrole
    2. Synonyms: 1-(2-bromo-4-fluorophenyl)-1H-pyrrole
    3. CAS NO:383137-41-5
    4. Molecular Formula: C10H7BrFN
    5. Molecular Weight: 240.0716832
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 383137-41-5.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 1-(2-bromo-4-fluorophenyl)-1H-pyrrole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(2-bromo-4-fluorophenyl)-1H-pyrrole(383137-41-5)
    11. EPA Substance Registry System: 1-(2-bromo-4-fluorophenyl)-1H-pyrrole(383137-41-5)

  • 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: 383137-41-5(Hazardous Substances Data)

383137-41-5 Usage

Uses

Used in Pharmaceutical Industry:
1-(2-bromo-4-fluorophenyl)-1H-pyrrole is used as an intermediate for the synthesis of various organic compounds, contributing to the development of new drugs. Its unique structural features make it a valuable building block in the pharmaceutical sector, where it can be utilized to create novel therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 1-(2-bromo-4-fluorophenyl)-1H-pyrrole serves as an intermediate for the synthesis of different organic compounds, which can be used to develop new agrochemicals. Its potential biological activities, such as antimicrobial and antifungal properties, make it a promising candidate for the creation of innovative products to address various agricultural challenges.
Used as Antimicrobial and Antifungal Agent:
1-(2-bromo-4-fluorophenyl)-1H-pyrrole is used as an antimicrobial and antifungal agent due to its inherent biological activities. These properties make it suitable for applications in various industries, including pharmaceuticals and agrochemicals, where it can be employed to combat microbial and fungal infections.

Check Digit Verification of cas no

The CAS Registry Mumber 383137-41-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,8,3,1,3 and 7 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 383137-41:
(8*3)+(7*8)+(6*3)+(5*1)+(4*3)+(3*7)+(2*4)+(1*1)=145
145 % 10 = 5
So 383137-41-5 is a valid CAS Registry Number.

383137-41-5SDS

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 1-(2-bromo-4-fluorophenyl)pyrrole

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:383137-41-5 SDS

383137-41-5Downstream Products

383137-41-5Relevant articles and documents

Palladium-catalyzed annulation of aryl heterocycles with strained alkenes

Hulcoop, David G.,Lautens, Mark

, p. 1761 - 1764 (2008/02/02)

An annulation reaction proceeding by the intermolecular addition of an arylpalladium(II) halide across a strained alkene, followed by an intramolecular C-H functionalization of a pendant heterocycle is described. A variety of polycyclic heterocycles have

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