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100191-85-3

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100191-85-3 Usage

Description

2-(4-Dimethylaminophenyl)furan is a chemical compound characterized by a furan ring with a 4-dimethylaminophenyl group attached at the 2 position. It is recognized for its distinctive properties and is widely utilized in the realms of chemistry and pharmaceuticals. 2-(4-Dimethylaminophenyl)furan serves as a valuable building block in organic synthesis, facilitating the construction of more intricate chemical structures. Moreover, its potential biological activity has garnered attention among medicinal chemists, making it a promising candidate for further research and development.

Uses

Used in Organic Synthesis:
2-(4-Dimethylaminophenyl)furan is used as a building block in organic synthesis for its ability to contribute to the formation of more complex chemical structures. Its unique structure allows for versatile reactions and the creation of a variety of compounds with different properties and applications.
Used in Pharmaceutical Research:
In the pharmaceutical industry, 2-(4-Dimethylaminophenyl)furan is used as a starting material for the development of new drugs. Its potential biological activity makes it an area of interest for researchers who are exploring its possible therapeutic uses and mechanisms of action.
Used in Chemical Reaction Studies:
2-(4-Dimethylaminophenyl)furan is utilized in the study of chemical reactions to understand its reactivity and the types of products that can be formed. This knowledge is crucial for optimizing synthetic routes and developing new methodologies in organic chemistry.
Used in Medicinal Chemistry:
2-(4-Dimethylaminophenyl)furan is employed in medicinal chemistry as a potential lead compound for the discovery of new pharmaceutical agents. Its structure and properties are investigated to identify how it may interact with biological targets and contribute to therapeutic effects.

Check Digit Verification of cas no

The CAS Registry Mumber 100191-85-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,1,9 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 100191-85:
(8*1)+(7*0)+(6*0)+(5*1)+(4*9)+(3*1)+(2*8)+(1*5)=73
73 % 10 = 3
So 100191-85-3 is a valid CAS Registry Number.

100191-85-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(furan-2-yl)-N,N-dimethylaniline

1.2 Other means of identification

Product number -
Other names 2-(4-Dimethylaminophenyl)furan

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:100191-85-3 SDS

100191-85-3Downstream Products

100191-85-3Relevant articles and documents

Impact of Five-membered Heterocyclic Rings on Photophysical Properties including Two-photon Absorption Character

Abe, Manabu,Chitose, Youhei,Lin, Tzu-Chau,Pham, Thuy Thi Thu,Tam, Tran Thi Thanh,Tseng, Wei-Lun

supporting information, p. 1810 - 1813 (2021/10/27)

A series of dipolar-type terphenyl derivatives 13 featuring an electron donor (p-NMe2C6H4 group) and acceptor (p-NO2C6H4 group) unit was synthesized and their photophysical properties were

Preparation of furans by palladium-catalyzed reaction of acylchromates and propargylic tosylates

Nakamura, Masaki,Yamane, Motoki,Sakurai, Hidehiro,Narasaka, Koichi

, p. 333 - 345 (2007/10/03)

Substituted furans are prepared by the palladium-catalyzed reaction of propargylic tosylates with acylchromates. The reaction is initiated by the oxidative additiion of propagylic tosylates to palladium(O) complexes to give 1,2-propadienylpalladium(II) co

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