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1345822-04-9

C19H25N3O3S is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1345822-04-9 Structure

  • Basic information

    1. Product Name: C19H25N3O3S
    2. Synonyms: C19H25N3O3S
    3. CAS NO:1345822-04-9
    4. Molecular Formula:
    5. Molecular Weight: 375.492
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1345822-04-9.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: C19H25N3O3S(CAS DataBase Reference)
    10. NIST Chemistry Reference: C19H25N3O3S(1345822-04-9)
    11. EPA Substance Registry System: C19H25N3O3S(1345822-04-9)

  • 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: 1345822-04-9(Hazardous Substances Data)

1345822-04-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1345822-04-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,4,5,8,2 and 2 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1345822-04:
(9*1)+(8*3)+(7*4)+(6*5)+(5*8)+(4*2)+(3*2)+(2*0)+(1*4)=149
149 % 10 = 9
So 1345822-04-9 is a valid CAS Registry Number.

1345822-04-9Relevant articles and documents

Synthesis and antimalarial activity of thioetherhydroxyethylsulfonamides, potential aspartyl protease inhibitors, Part 3

Vellasco Junior, Walcimar T.,Guedes, Guilherme P.,Vasconcelos, Thatyana R.A.,Vaz, Maria G.F.,De Souza, Marcus V.N.,Krettli, Antoniana U.,Krettli, Luisa G.,Aguiar, Anna Caroline C.,Gomes, Claudia R.B.,Cunico, Wilson

, p. 5688 - 5693 (2011)

A series of novel thioetherhydroxyethylsulfonamide derivatives has been synthesized from the coupling of intermediates 3-amino-4-phenyl-1- thioetherazine-butan-2-oles 6,7 with arenesulfonyl chlorides in good yields. Characterizations of products were achieved by NMR techniques and specifically for compound 8e by X-ray crystallography. Preliminary results of antimalarial activity in vitro against the Plasmodium falciparum W2 clone (chloroquine resistant and mefloquine sensitive) showed moderate activity for hydroxyethylsulfonamide 8f. In addition, none of the compounds tested showed cytotoxicity at high concentration tested against HepG2 and BGM cell lines.

Antibacterial activity of thioetherhydroxyethylsulfonamide derivatives

Vellasco Jr., Walcimar T.,Guedes, Guilherme P.,Facchinetti, Victor,Vasconcelos, Thatyana R.A.,Vaz, Maria G.F.,Cunico, Wilson,De Souza, Marcus V.N.,De Paula, Geraldo R.,Fleming, Maria E.C.K.,Gomes, Claudia R.B.

, p. 271 - 276 (2014/05/06)

Thioetherhydroxyethylsulfonamide derivatives were synthesized and evaluated for their in vitro antibacterial activity against Escherichia coli (ATCC 25922), Pseudomonas aeruginosa (ATCC 27853) and Staphylococcus aureus (ATCC 25923). Results have shown tha

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