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1-(2-BROMO-4-METHYLPHENYL)-1H-PYRROLE-2-CARBALDEHYDE is a pyrrole derivative with the molecular formula C12H10BrNO, featuring a bromine-substituted phenyl group and a carbaldehyde functional group. 1-(2-BROMO-4-METHYLPHENYL)-1H-PYRROLE-2-CARBALDEHYDE is known for its versatile chemical properties, making it a significant component in the development of advanced materials and pharmaceuticals.

142045-46-3

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142045-46-3 Usage

Uses

Used in Pharmaceutical Research:
1-(2-BROMO-4-METHYLPHENYL)-1H-PYRROLE-2-CARBALDEHYDE is used as a building block in pharmaceutical research for the development of new drugs and biologically active molecules. Its unique structure and functional groups contribute to the creation of novel compounds with potential therapeutic applications.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(2-BROMO-4-METHYLPHENYL)-1H-PYRROLE-2-CARBALDEHYDE serves as an essential component for constructing complex organic molecules. Its reactivity and structural diversity allow for the synthesis of a wide range of compounds with various applications.
Used in Materials Science:
1-(2-BROMO-4-METHYLPHENYL)-1H-PYRROLE-2-CARBALDEHYDE has potential applications in materials science, where its chemical properties can be utilized to develop new materials with specific properties. These materials could be used in various industries, such as electronics, aerospace, or automotive, depending on the desired characteristics.
Used in Industrial Chemical Processes:
1-(2-BROMO-4-METHYLPHENYL)-1H-PYRROLE-2-CARBALDEHYDE may also find use in industrial chemical processes, where its unique properties can be harnessed to improve the efficiency or yield of certain reactions. This could lead to more sustainable and cost-effective production methods in the chemical industry.

Check Digit Verification of cas no

The CAS Registry Mumber 142045-46-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,0,4 and 5 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 142045-46:
(8*1)+(7*4)+(6*2)+(5*0)+(4*4)+(3*5)+(2*4)+(1*6)=93
93 % 10 = 3
So 142045-46-3 is a valid CAS Registry Number.

142045-46-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(2-BROMO-4-METHYLPHENYL)-1H-PYRROLE-2-CARBALDEHYDE

1.2 Other means of identification

Product number -
Other names 1-(2-Bromo-4-methylphenyl)pyrrole-2-carbaldehyde

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:142045-46-3 SDS

142045-46-3Downstream Products

142045-46-3Relevant academic research and scientific papers

Construction of benzo-fused indolizines, pyrrolo[1,2-a]quinolines via alkyne-carbonyl metathesis

Nayak, Maloy,Kim, Ikyon

, p. 9697 - 9708 (2015/09/28)

The strategic use of a sequential Sonogashira coupling/intramolecular alkyne-carbonyl metathesis process for the synthesis of a pyridine ring from 1-(2-haloaryl)-1H-pyrrole-2-carbaldehydes allowed ready access to diverse novel benzo-fused indolizines, pyr

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

ANGIOTENSIN II ANTAGONIZING HETEROCYCLIC DERIVATIVES

-

, (2008/06/13)

The invention relates to compounds of the formula STR1 wherein STR2 represents a condensed or uncondensed imidazolyl ring and the rest of the variables are as defined in the specification. They are angiotensin II antagonists useful for treating hypertension, etc..

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