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

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  • 33144-95-5 Structure
  • Basic information

    1. Product Name: benzoyl-selenosemicarbazide
    2. Synonyms: benzoyl-selenosemicarbazide
    3. CAS NO:33144-95-5
    4. Molecular Formula:
    5. Molecular Weight: 242.139
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 33144-95-5.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: benzoyl-selenosemicarbazide(CAS DataBase Reference)
    10. NIST Chemistry Reference: benzoyl-selenosemicarbazide(33144-95-5)
    11. EPA Substance Registry System: benzoyl-selenosemicarbazide(33144-95-5)
  • 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: 33144-95-5(Hazardous Substances Data)

33144-95-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33144-95-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,1,4 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 33144-95:
(7*3)+(6*3)+(5*1)+(4*4)+(3*4)+(2*9)+(1*5)=95
95 % 10 = 5
So 33144-95-5 is a valid CAS Registry Number.

33144-95-5Downstream Products

33144-95-5Relevant articles and documents

Heterocycles 23: Synthesis, characterization and anticancer activity of new hydrazinoselenazole derivatives

Zaharia, Valentin,Ignat, Adriana,Ngameni, Bathelemy,Kuete, Victor,Moungang, Marlyse L.,Fokunang, Charles N.,Vasilescu, Mihai,Palibroda, Nicolae,Cristea, Castelia,Silaghi-Dumitrescu, Luminita,Ngadjui, Bonaventure T.

, p. 5670 - 5679 (2013/11/06)

A series of novel functionalized 1,3-selenazole was synthesized by Hantzsch-type condensation reaction and evaluated for their in vitro cytotoxic activity against two human cancer cell lines. The structures of the synthesized selenosemicarbazones and func

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