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59908-32-6

1(2H)-Phthalazinethione, 4-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 59908-32-6 Structure

  • Basic information

    1. Product Name: 1(2H)-Phthalazinethione, 4-(phenylmethyl)-
    2. Synonyms:
    3. CAS NO:59908-32-6
    4. Molecular Formula: C15H12N2S
    5. Molecular Weight: 252.34
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 59908-32-6.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(2H)-Phthalazinethione, 4-(phenylmethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1(2H)-Phthalazinethione, 4-(phenylmethyl)-(59908-32-6)
    11. EPA Substance Registry System: 1(2H)-Phthalazinethione, 4-(phenylmethyl)-(59908-32-6)

  • 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: 59908-32-6(Hazardous Substances Data)

59908-32-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 59908-32-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,9,0 and 8 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 59908-32:
(7*5)+(6*9)+(5*9)+(4*0)+(3*8)+(2*3)+(1*2)=166
166 % 10 = 6
So 59908-32-6 is a valid CAS Registry Number.

59908-32-6Relevant articles and documents

Design and synthesis of new phthalazinone derivatives containing benzyl moiety with anticipated antitumor activity

Marzouk, Magda Ismail,Shaker, Soheir Ahmad,Hafiz, Aisha Ali Abdel,El-Baghdady, Khaled Zakaria

, p. 239 - 251 (2016)

The acetohydrazide derivative reacted with carbon electrophiles such as acid chlorides, acetylacetone, ethyl acetoacetate and aromatic aldehydes to give some interesting heterocyclic compounds. The hydrazide derivative reacted with acetophenone which in turn underwent Vielsmeier-Haack reaction. Also, the phthalazinethione has been synthesized and its behavior towards hydrazine hydrate, oxidizing agent and ethyl chloroacetate has been investigated. The newly synthesized compounds were characterized by spectroscopic data. The antimicrobial, the cytotoxic, and the antioxidant activities of some of the synthesized products were evaluated. Some of the tested compounds showed very strong cytotoxic activity with respect to the standard.

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