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CAS

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1569303-97-4

1-phenyl-5-(3,4,5-trimethoxyphenylthio)-1H-tetrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1569303-97-4 Structure

  • Basic information

    1. Product Name: 1-phenyl-5-(3,4,5-trimethoxyphenylthio)-1H-tetrazole
    2. Synonyms:
    3. CAS NO:1569303-97-4
    4. Molecular Formula:
    5. Molecular Weight: 344.394
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1569303-97-4.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: 1-phenyl-5-(3,4,5-trimethoxyphenylthio)-1H-tetrazole(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-phenyl-5-(3,4,5-trimethoxyphenylthio)-1H-tetrazole(1569303-97-4)
    11. EPA Substance Registry System: 1-phenyl-5-(3,4,5-trimethoxyphenylthio)-1H-tetrazole(1569303-97-4)

  • 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: 1569303-97-4(Hazardous Substances Data)

1569303-97-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1569303-97-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,6,9,3,0 and 3 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1569303-97:
(9*1)+(8*5)+(7*6)+(6*9)+(5*3)+(4*0)+(3*3)+(2*9)+(1*7)=194
194 % 10 = 4
So 1569303-97-4 is a valid CAS Registry Number.

1569303-97-4Downstream Products

1569303-97-4Relevant articles and documents

AROMATIC SULFIDE COMPOUNDS AND METHODS AND USE THEREOF

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Paragraph 0168; 0190, (2015/11/03)

Described herein, inter alia, are aromatic sulfide compositions and methods for treating or preventing cancer using the same.

Diaryl and heteroaryl sulfides: Synthesis via sulfenyl chlorides and evaluation as selective anti-breast-cancer agents

Yonova, Ivelina M.,Osborne, Charlotte A.,Morrissette, Naomi S.,Jarvo, Elizabeth R.

, p. 1947 - 1953 (2014/04/03)

A mild protocol for the synthesis of diaryl and heteroaryl sulfides is described. In a one-pot procedure, thiols are converted to sulfenyl chlorides and reacted with arylzinc reagents. This method tolerates functional groups including aryl fluorides and chlorides, ketones, as well as N-heterocycles including pyrimidines, imidazoles, tetrazoles, and oxadiazoles. Two compounds synthesized by this method exhibited selective activity against the MCF-7 breast cancer cell line in the micromolar range.

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