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4(3H)-Quinazolinethione, 3-amino-2-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13961-55-2 Structure
  • Basic information

    1. Product Name: 4(3H)-Quinazolinethione, 3-amino-2-phenyl-
    2. Synonyms:
    3. CAS NO:13961-55-2
    4. Molecular Formula: C14H11N3S
    5. Molecular Weight: 253.327
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13961-55-2.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: 4(3H)-Quinazolinethione, 3-amino-2-phenyl-(CAS DataBase Reference)
    10. NIST Chemistry Reference: 4(3H)-Quinazolinethione, 3-amino-2-phenyl-(13961-55-2)
    11. EPA Substance Registry System: 4(3H)-Quinazolinethione, 3-amino-2-phenyl-(13961-55-2)
  • 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: 13961-55-2(Hazardous Substances Data)

13961-55-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13961-55-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,9,6 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 13961-55:
(7*1)+(6*3)+(5*9)+(4*6)+(3*1)+(2*5)+(1*5)=112
112 % 10 = 2
So 13961-55-2 is a valid CAS Registry Number.

13961-55-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-amino-2-phenylquinazoline-4-thione

1.2 Other means of identification

Product number -
Other names 3-amino-2-phenyl-4-thioxo-3,4-dihydroquinazoline

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:13961-55-2 SDS

13961-55-2Upstream product

13961-55-2Relevant articles and documents

Quinazolinone platinum metal complexes: In silico design, synthesis and evaluation of anticancer activity

Sawant, Sanjay D.,Sahu, Megha,Nerkar, Amit G.

, p. 2164 - 2170 (2018)

Dihydrofolate reductase (DHFR) has been explored as a target for the development of agents for wide variety of human diseases, including cancer, autoimmune and infectious diseases. Several metal complexes are being used in management of cancer. The square planar Pt(II) complex, cis PtCl2(NH3)2 turned out to be even more effective at forcing filamentous growth. Cisplatin is an inorganic heavy metal complex that has activity similar to cell-cycle-phase-nonspecific alkylating agents such as cyclophosphamide and some other Ni and Cu metal complexes. It produces intrastrand DNA cross-link and form DNA adducts, thus inhibiting the synthesis of DNA, RNA and proteins preferentially. in silico Screening of platinum metal complexes was performed by Vlife MDS 4.3 software. In this procedure, selection of molecule, selection of PDB, optimization of PDB and docking of molecules was carried out. Synthesis of metal complexes was done by multi component reaction method. Platinum metal complexes of quinazolinone Schiff bases prioritized by in silico studies were characterized by IR, TLC, NMR, XRD, FESEM and some physico-chemical parameters. Prioritized molecules were further evaluated by in vitro anticancer cell line assay on ten cell lines with adriamycin as standard. The results showed that the platinum metal complexes of qunazolinone Schiff bases can be potential anticancer agents through DHFR inhibitory mechanism.

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