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1H-Pyrrole-2-carboxaldehyde, 5-(4-methoxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

431039-10-0

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431039-10-0 Usage

Chemical class

Pyrroles

Derivative

Pyrrole carboxaldehyde

Substituent group

5-(4-methoxyphenyl)

Usage

Reagent and intermediate for the synthesis of pharmaceuticals and organic molecules

Aromatic properties

Known for its characteristic odor and aromatic properties

Building block

Used for the synthesis of heterocyclic compounds

Value

Valuable component in the development of novel drugs and biologically active molecules

Check Digit Verification of cas no

The CAS Registry Mumber 431039-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,1,0,3 and 9 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 431039-10:
(8*4)+(7*3)+(6*1)+(5*0)+(4*3)+(3*9)+(2*1)+(1*0)=100
100 % 10 = 0
So 431039-10-0 is a valid CAS Registry Number.

431039-10-0Downstream Products

431039-10-0Relevant articles and documents

Isomer-Specific Hydrogen Bonding as a Design Principle for Bidirectionally Quantitative and Redshifted Hemithioindigo Photoswitches

Zweig, Joshua E.,Newhouse, Timothy R.

, p. 10956 - 10959 (2017)

A new class of bidirectionally quantitative photoswitches based on the hemithioindigo (HTI) scaffold is reported. Incorporation of a pyrrole hydrogen-bond donor leads to a bathochromic shift allowing for quantitative bidirectional isomerization. Additionally, extending conjugation from the electron-rich pyrrole results in quantitative visible-light photoswitches, as well as photoswitches that isomerize with red and near-infrared light. The presence of the hydrogen bond leading to the observed redshift is supported by computational and spectroscopic evidence.

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