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332150-33-1

6-bromo-2-methyl-4-quinolinyl hydrosulfide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 332150-33-1 Structure

  • Basic information

    1. Product Name: 6-bromo-2-methyl-4-quinolinyl hydrosulfide
    2. Synonyms: 6-bromo-2-methyl-4-quinolinyl hydrosulfide
    3. CAS NO:332150-33-1
    4. Molecular Formula: C10H8BrNS
    5. Molecular Weight: 254.14622
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 332150-33-1.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 6-bromo-2-methyl-4-quinolinyl hydrosulfide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-bromo-2-methyl-4-quinolinyl hydrosulfide(332150-33-1)
    11. EPA Substance Registry System: 6-bromo-2-methyl-4-quinolinyl hydrosulfide(332150-33-1)

  • 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: 332150-33-1(Hazardous Substances Data)

332150-33-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 332150-33-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,1,5 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 332150-33:
(8*3)+(7*3)+(6*2)+(5*1)+(4*5)+(3*0)+(2*3)+(1*3)=91
91 % 10 = 1
So 332150-33-1 is a valid CAS Registry Number.

332150-33-1Downstream Products

332150-33-1Relevant articles and documents

Synthesis of substituted 2-methyl-4-quinolyl isothiocyanates and 4-mercaptoquinolines

Avetisyan,Aleksanyan,Ambartsumyan

, p. 769 - 771 (2005)

Synthesis was performed of substituted 2-methyl-4-quinoline thiouronium salts by reaction of 2-methyl-4-chloroquinolines with thiourea. The alkaline hydrolysis of these salts afforded the corresponding 2-methyl-4-quinolyl- isothiocyanates and 2-methyl-4-mercaptoquinolines. 2005 Pleiades Publishing, Inc.

Synthesis and antimicrobial evaluation of some new quinaldine derivatives

Al-Abdullah, Ebtehal S.,Haress, Nadia G.,Haiba, Mogedda E.,Mohamed, Neama A.,Mahmoud, Amany Z.

, p. 1453 - 1464 (2017/10/23)

A new series of quinoline derivatives incorporated to glycosides and biologically active heterocyclic moieties were synthesized starting with 6-bromo-4-hydroxyquinaldine (6-bromo-4-hydroxy-2-methylquino-line) compound 1. Some of the synthesized compounds were evaluated for their antibacterial and antifungal activities. Most of the tested compounds exhibited potential antibacterial activity against Gram-positive bacteria, the detailed synthesis, spectroscopic data, antibacterial and antifungal evaluation of the synthesized compounds are reported.

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