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41422-62-2

sodium 4-methoxyphenylselenolate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 41422-62-2 Structure

  • Basic information

    1. Product Name: sodium 4-methoxyphenylselenolate
    2. Synonyms: sodium 4-methoxyphenylselenolate
    3. CAS NO:41422-62-2
    4. Molecular Formula:
    5. Molecular Weight: 209.082
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 41422-62-2.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: sodium 4-methoxyphenylselenolate(CAS DataBase Reference)
    10. NIST Chemistry Reference: sodium 4-methoxyphenylselenolate(41422-62-2)
    11. EPA Substance Registry System: sodium 4-methoxyphenylselenolate(41422-62-2)

  • 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: 41422-62-2(Hazardous Substances Data)

41422-62-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 41422-62-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,1,4,2 and 2 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 41422-62:
(7*4)+(6*1)+(5*4)+(4*2)+(3*2)+(2*6)+(1*2)=82
82 % 10 = 2
So 41422-62-2 is a valid CAS Registry Number.

41422-62-2Relevant articles and documents

Discovery of new 2, 5-disubstituted 1,3-selenazoles as selective human carbonic anhydrase IX inhibitors with potent anti-tumor activity

Angeli, Andrea,Trallori, Elena,Ferraroni, Marta,Di Cesare Mannelli, Lorenzo,Ghelardini, Carla,Supuran, Claudiu T.

, p. 1214 - 1222 (2018)

A series of disubstituted selenazole derivatives was synthetized and evaluated as carbonic anhydrase (CA, EC 4.2.1.1) inhibitors against the human (h) isoforms hCA I, II, IV, VA, VB and IX, involved in a variety of diseases including glaucoma, retinitis pigmentosa, epilepsy, arthritis and tumors. The investigated compounds showed potent inhibition against the tumor-associated transmembrane hCA IX, with KIs in the subnanomolar – low nanomolar range, and were evaluated for their effects on cell viability against the human prostate (PC3) and breast (MDA-MB-231) cancer cell lines, showing effective anti-tumor activity. These selenazoles are interesting leads for the development of new, isoform-selective CA IX inhibitors.

Facile synthesis of mixed O, S or Se bearing hexasubstituted benzenes and their potential as Cu(ii) ion probe

Kumar, Abhishek,Yadav, Mantesh K.,Singh, Jagriti,Singh, Jai Deo,Butcher, Ray J.

, p. 5627 - 5636 (2019/05/10)

The present study offers a facile route for the synthesis of unsymmetrical hexasubstituted benzenes bearing alternate heteroatoms (O, S and Se) with the formula [1,3,5-(RSeCH2)3-2,4,6-(R′ECH2)3C6] (E

Synthesis and conformational analysis of 2-arylseleno-1,3-dithianes. Crystal and molecular structure of 2-(4-methoxyphenylseleno)- and 2-(4-trifluoromethylphenylseleno)-1,3-dithiane

Pinto, B. Mario,Sandoval-Ramirez, Jesus,Sharma, R. Dev,Willis, Anthony C.,Einstein, Frederick W. B.

, p. 732 - 738 (2007/10/02)

The synthesis of 2-(4-methoxyphenylseleno)-1,3-dithiane 3 and 2-(4-trifluoromethylphenylseleno)-1,3-dithiane 5 from 2-chloro-1,3-dithiane 1 and the corresponding sodium arylselenolates is described.Nuclear magnetic resonance spectroscopic investigation of

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