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3-(4-BROMO-PHENYL)-1H-PYRROLE is a chemical compound with a molecular formula of C10H8BrN. It is a pyrrole derivative with a bromine atom attached to the fourth position of the phenyl group. 3-(4-BROMO-PHENYL)-1H-PYRROLE is commonly used as a building block in organic synthesis and medicinal chemistry due to its potential biological activities and pharmacological properties.

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  • 848006-35-9 Structure
  • Basic information

    1. Product Name: 3-(4-BROMO-PHENYL)-1H-PYRROLE
    2. Synonyms: 3-(4-BROMO-PHENYL)-1H-PYRROLE
    3. CAS NO:848006-35-9
    4. Molecular Formula: C10H8BrN
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 848006-35-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 355.389°C at 760 mmHg
    3. Flash Point: 168.734°C
    4. Appearance: /
    5. Density: 1.488g/cm3
    6. Vapor Pressure: 0mmHg at 25°C
    7. Refractive Index: 1.628
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: 3-(4-BROMO-PHENYL)-1H-PYRROLE(CAS DataBase Reference)
    11. NIST Chemistry Reference: 3-(4-BROMO-PHENYL)-1H-PYRROLE(848006-35-9)
    12. EPA Substance Registry System: 3-(4-BROMO-PHENYL)-1H-PYRROLE(848006-35-9)
  • 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: 848006-35-9(Hazardous Substances Data)

848006-35-9 Usage

Uses

Used in Organic Synthesis:
3-(4-BROMO-PHENYL)-1H-PYRROLE is used as a building block for the synthesis of various complex organic compounds. Its unique structure allows for the creation of a wide range of molecules with diverse applications.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 3-(4-BROMO-PHENYL)-1H-PYRROLE is used as a starting material for the development of new pharmaceuticals. Its potential biological activities and pharmacological properties make it a promising candidate for the treatment of various diseases.
Used in Antifungal Applications:
3-(4-BROMO-PHENYL)-1H-PYRROLE has been studied for its antifungal effects, making it a potential candidate for use in the development of antifungal agents to combat fungal infections.
Used in Antitumor Applications:
3-(4-BROMO-PHENYL)-1H-PYRROLE has also been investigated for its antitumor effects, indicating its potential use in the development of cancer treatments and therapies.
Used in Material Science:
3-(4-BROMO-PHENYL)-1H-PYRROLE may be utilized in the development of new materials, taking advantage of its unique chemical properties to create innovative products in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 848006-35-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,4,8,0,0 and 6 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 848006-35:
(8*8)+(7*4)+(6*8)+(5*0)+(4*0)+(3*6)+(2*3)+(1*5)=169
169 % 10 = 9
So 848006-35-9 is a valid CAS Registry Number.
InChI:InChI=1/C10H8BrN/c11-10-3-1-8(2-4-10)9-5-6-12-7-9/h1-7,12H

848006-35-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(4-bromophenyl)-1H-pyrrole

1.2 Other means of identification

Product number -
Other names GL-1063

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:848006-35-9 SDS

848006-35-9Downstream Products

848006-35-9Relevant articles and documents

Metal-Free Directed C?H Borylation of Pyrroles

Wang, Zheng-Jun,Chen, Xiangyang,Wu, Lei,Wong, Jonathan J.,Liang, Yong,Zhao, Yue,Houk, Kendall N.,Shi, Zhuangzhi

, p. 8500 - 8504 (2021/03/16)

Robust strategies to enable the rapid construction of complex organoboronates in selective, practical, low-cost, and environmentally friendly modes remain conspicuously underdeveloped. Here, we develop a general strategy for the site-selective C?H borylation of pyrroles by using only BBr3 directed by pivaloyl groups, avoiding the use of any metal. The site-selectivity is generally dominated by chelation and electronic effects, thus forming diverse C2-borylated pyrroles against the steric effect. The formed products can readily engage in downstream transformations, enabling a step-economic process to access drugs such as Lipitor. DFT calculations (wB97X-D) demonstrate the preferred positional selectivity of this reaction.

METHODS FOR MAKING BACTERIOCHLORIN MACROCYCLES COMPRISING AN ANNULATED ISOCYCLIC RING AND RELATED COMPOUNDS

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Page/Page column 80; 100; 101, (2018/06/21)

Described herein are bacteriochlorins comprising an annulated isocyclic ring. Also described are methods and intermediates for the synthesis of bacteriochlorins comprising an annulated isocyclic ring, and methods of using such bacteriochlorins for, among

Construction of the Bacteriochlorin Macrocycle with Concomitant Nazarov Cyclization To Form the Annulated Isocyclic Ring: Analogues of Bacteriochlorophyll a

Zhang, Shaofei,Lindsey, Jonathan S.

, p. 2489 - 2504 (2017/03/14)

Bacteriochlorophylls contain a bacteriochlorin macrocycle bearing an annulated fifth ring. The fifth ring, termed the isocyclic ring or ring E, is equipped with 131-oxo and 132-carbomethoxy substituents. Herein, a general route to st

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