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1-(4-ETHOXY-PHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBALDEHYDE is a chemical compound characterized by its unique structure, which includes a pyrrole ring, an aldehyde group, an ethoxy group, and two methyl groups. 1-(4-ETHOXY-PHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBALDEHYDE is widely utilized in organic synthesis and pharmaceutical research as a versatile building block for a variety of chemical reactions. Its structural features and reactivity contribute to its potential applications in drug discovery and development, as well as in the creation of new materials and as a research tool in organic chemistry.

347331-41-3

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347331-41-3 Usage

Uses

Used in Pharmaceutical Research:
1-(4-ETHOXY-PHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBALDEHYDE is used as a building block for the synthesis of various pharmaceutical compounds due to its structural features and reactivity. Its ability to participate in a range of chemical reactions makes it a valuable component in the development of new drugs.
Used in Organic Synthesis:
In the field of organic synthesis, 1-(4-ETHOXY-PHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBALDEHYDE serves as a key intermediate for the creation of diverse chemical products. Its unique structure allows for the formation of various derivatives, expanding the scope of possible applications.
Used in Drug Discovery and Development:
1-(4-ETHOXY-PHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBALDEHYDE is used as a starting material in drug discovery and development processes. Its potential applications in this field are attributed to its structural features, which make it a promising candidate for the creation of novel therapeutic agents.
Used in Material Science:
1-(4-ETHOXY-PHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBALDEHYDE may also have uses in the development of new materials, capitalizing on its unique chemical structure and reactivity to create innovative products with potential applications in various industries.
Used as a Research Tool in Organic Chemistry:
1-(4-ETHOXY-PHENYL)-2,5-DIMETHYL-1H-PYRROLE-3-CARBALDEHYDE is employed as a research tool in organic chemistry, enabling scientists to study its properties and reactivity. This helps in understanding the underlying mechanisms of various chemical reactions and contributes to the advancement of the field.

Check Digit Verification of cas no

The CAS Registry Mumber 347331-41-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,7,3,3 and 1 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 347331-41:
(8*3)+(7*4)+(6*7)+(5*3)+(4*3)+(3*1)+(2*4)+(1*1)=133
133 % 10 = 3
So 347331-41-3 is a valid CAS Registry Number.
InChI:InChI=1/C15H17NO2/c1-4-18-15-7-5-14(6-8-15)16-11(2)9-13(10-17)12(16)3/h5-10H,4H2,1-3H3

347331-41-3SDS

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 1-(4-ethoxyphenyl)-2,5-dimethylpyrrole-3-carbaldehyde

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

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More Details:347331-41-3 SDS

347331-41-3Downstream Products

347331-41-3Relevant academic research and scientific papers

Synthesis and biological evaluation of 6-aryl-6H-pyrrolo[3,4-d]pyridazine derivatives: High-affinity ligands to the α2δ subunit of voltage gated calcium channels

Stearns, Brian A.,Anker, Naomi,Arruda, Jeannie M.,Campbell, Brian T.,Chen, Chixu,Cramer, Merryl,Hu, Tao,Jiang, Xiaohui,Park, Kenneth,Ren, Kun Kun,Sablad, Marciano,Santini, Angelina,Schaffhauser, Herve,Urban, Mark O.,Munoz, Benito

, p. 1295 - 1298 (2007/10/03)

A novel class of 6-aryl-6H-pyrrolo[3,4-d]pyridazine ligands for the α2δ subunit of voltage-gated calcium channels has been described. Substitutions in the aryl ring of the molecule were generally not tolerated, and resulted in diminished bindin

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