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  • 20406-60-4 Structure
  • Basic information

    1. Product Name: Mipimazole
    2. Synonyms: Mipimazole;1-Isopropyl-2-imidazolidinethione;1-Isopropylimidazolidine-2-thione;Centimizone
    3. CAS NO:20406-60-4
    4. Molecular Formula: C6H12N2S
    5. Molecular Weight: 144.241
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 20406-60-4.mol
  • Chemical Properties

    1. Melting Point: 166 °C
    2. Boiling Point: 188.7°Cat760mmHg
    3. Flash Point: 67.9°C
    4. Appearance: /
    5. Density: 1.11g/cm3
    6. Vapor Pressure: 0.591mmHg at 25°C
    7. Refractive Index: 1.568
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. PKA: 14.84±0.20(Predicted)
    11. CAS DataBase Reference: Mipimazole(CAS DataBase Reference)
    12. NIST Chemistry Reference: Mipimazole(20406-60-4)
    13. EPA Substance Registry System: Mipimazole(20406-60-4)
  • 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: 20406-60-4(Hazardous Substances Data)

20406-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 20406-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,0 and 6 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 20406-60:
(7*2)+(6*0)+(5*4)+(4*0)+(3*6)+(2*6)+(1*0)=64
64 % 10 = 4
So 20406-60-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N2S/c1-5(2)8-4-3-7-6(8)9/h5H,3-4H2,1-2H3,(H,7,9)

20406-60-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-propan-2-ylimidazolidine-2-thione

1.2 Other means of identification

Product number -
Other names 1-isopropylimidazolidine-2-thione

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:20406-60-4 SDS

20406-60-4Downstream Products

20406-60-4Relevant articles and documents

Precursor reaction kinetics control compositional grading and size of CdSe1-: XSx nanocrystal heterostructures

Hamachi, Leslie S.,Yang, Haoran,Jen-La Plante, Ilan,Saenz, Natalie,Qian, Kevin,Campos, Michael P.,Cleveland, Gregory T.,Rreza, Iva,Oza, Aisha,Walravens, Willem,Chan, Emory M.,Hens, Zeger,Crowther, Andrew C.,Owen, Jonathan S.

, p. 6539 - 6552 (2019/07/10)

We report a method to control the composition and microstructure of CdSe1-xSx nanocrystals by the simultaneous injection of sulfide and selenide precursors into a solution of cadmium oleate and oleic acid at 240 °C. Pairs of substituted thio- and selenoureas were selected from a library of compounds with conversion reaction reactivity exponents (kE) spanning 1.3 × 10-5 s-1 to 2.0 × 10-1 s-1. Depending on the relative reactivity (kSe/kS), core/shell and alloyed architectures were obtained. Growth of a thick outer CdS shell using a syringe pump method provides gram quantities of brightly photoluminescent quantum dots (PLQY = 67 to 90%) in a single reaction vessel. Kinetics simulations predict that relative precursor reactivity ratios of less than 10 result in alloyed compositions, while larger reactivity differences lead to abrupt interfaces. CdSe1-xSx alloys (kSe/kS = 2.4) display two longitudinal optical phonon modes with composition dependent frequencies characteristic of the alloy microstructure. When one precursor is more reactive than the other, its conversion reactivity and mole fraction control the number of nuclei, the final nanocrystal size at full conversion, and the elemental composition. The utility of controlled reactivity for adjusting alloy microstructure is discussed.

Platinum(II) complexes with thione ligands and methods thereof

-

Page/Page column 20, (2016/11/21)

Platinum(II) complexes having thione-based heterocyclic ligands as anticancer agents. The central platinum atom is coordinated by four of the ligands, each having a five-, six- or seven-membered heterocyclic ring with two nitrogen atoms at positions 1 and 3 of the ring and a thiocarbonyl group at position 2. Pharmaceutical compositions incorporated the platinum(II) complexes, methods of synthesizing the complexes and methods of treating cancers with the complexes or pharmaceutical compositions thereof are also described.

Tetrakis(thione)platinum(II) complexes: Synthesis, spectroscopic characterization, crystal structures, and in vitro cytotoxicity

Mustafa, A. Zainelabdeen A.,Monim-ul-Mehboob,Jomaa,Altaf,Fettouhi,Isab,Wazeer,Stoeckli-Evans,Bhatia,Dhuna

, p. 3511 - 3524 (2015/09/28)

A new series of platinum(II) complexes based on thione ligands with general formula [Pt(thione)4]X2 (X- = Cl-, NO3-) has been synthesized and characterized using CHNS elemental analysis, infrared, 1H and 13C solution-state NMR as well as 13C and 15N solid-state NMR spectroscopy, and X-ray crystallography. The spectroscopic methods confirm the coordination of Pt(II) with thiocarbonyl groups via sulfur of the thione ligands. The X-ray structures showed a distorted square planar geometry for 1, [Pt(MeImt)4]Cl2 (MeImt = N-Methylimidazolidine-2-thione) while the hydrogen bonding interactions in 7, [Pt(iPrImt)4](NO3)2·0.6(H2O) induce a bent see-saw distortion relative to the ideal square planar geometry. The in vitro cytotoxicity studies showed that 2, [Pt(EtImt)4]Cl2 is generally the most effective, a two-fold better cytotoxic agent than cisplatin and carboplatin against MCF7 (human breast cancer).

Solid-phase synthesis of 2-imidazolidinethiones via Mitsunobu reaction of N-(2-hydroxyethyl)thioureas

Jeon, Hyun Suk,Yoo, Je Hwa,Kim, Jae Nyoung,Kim, Taek Hyeon

, p. 439 - 441 (2008/02/03)

This letter reports the solid-phase synthesis of 2-imidazolidinethiones via the N-cyclization of N-(2-hydroxyethyl)thioureas using the Mitsunobu reaction in good yield and purity. This process employed the reductive amination of an ArgoGel-MB-CHO resin to

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