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3-methyl-2,4-diphenyl-1,3-thiazol-3-ium-5-thiolate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 15995-22-9 Structure
  • Basic information

    1. Product Name: 3-methyl-2,4-diphenyl-1,3-thiazol-3-ium-5-thiolate
    2. Synonyms: 3-methyl-2,4-diphenyl-1,3-thiazol-3-ium-5-thiolate
    3. CAS NO:15995-22-9
    4. Molecular Formula: C16H13NS2
    5. Molecular Weight: 283.41112
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 15995-22-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: 3-methyl-2,4-diphenyl-1,3-thiazol-3-ium-5-thiolate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-methyl-2,4-diphenyl-1,3-thiazol-3-ium-5-thiolate(15995-22-9)
    11. EPA Substance Registry System: 3-methyl-2,4-diphenyl-1,3-thiazol-3-ium-5-thiolate(15995-22-9)
  • 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: 15995-22-9(Hazardous Substances Data)

15995-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15995-22-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,9,9 and 5 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 15995-22:
(7*1)+(6*5)+(5*9)+(4*9)+(3*5)+(2*2)+(1*2)=139
139 % 10 = 9
So 15995-22-9 is a valid CAS Registry Number.

15995-22-9Relevant articles and documents

Influence of the aromatic substitutes in the thermal and kinetic behavior of mesoionic compounds of the 1,3-thiazole-5-tiolate system

de Morais, Soraya Alves,da Silva Morais, Crislene Rodrigues,Filho, Petr?nio Filgueiras de Athayde,Lira, Bruno Freitas,Souza, Marcos Antonio feitosa de

experimental part, p. 598 - 602 (2010/08/21)

In this work, three mesoionic compounds of the 1,3-thiazole-5-tiolat system were studied, derived from amino acids of the glycerin through 1,3-dipolar cyclo-addition/reversion reaction. The mesoionic compounds were characterized as: MI-1 (mesoionic 2-(4-chlorophenyl)-3-methyl-4-phenyl-1,3-thiazole-5-tiolat); MI-2 (mesoionic 2-(4-chlorophenyl)-3-methyl-4-(4-isopropylphenyl)-1,3-thiazole-5-tiolat) and MI-3 (Mesoionic 2-(4-clorophenyl)-3-methyl-4-(methoxyphenyl)-1,3-thiazole-5-tiolate). These compounds were characterized by infrared spectroscopy (IR), nuclear magnetic resonance (NMR), thermogravimetry (TG) and differential scanning calorimeter (DSC). Also, the kinetic study of the thermal decomposition by non-isothermal thermogravimetry has been realized, presenting, the kinetic and thermal behavior of these compounds. The results of the spectroscopic analysis confirmed the structure of the synthesized mesoionic compounds. The DSC curves of the mesoionic compounds MI-1, MI-2, and MI-3 indicated the fusion of two of them followed by a subsequent decomposition. The TG/DTG curves showed that the decomposition of the mesoionic compounds MI-1, MI-2 and MI-3 occurred in several steps.

Synthesis, characterization and crystallographic studies of three 2-aryl-3-methyl-4-aryl-1,3-thiazolium-5-thiolates

De Athayde-Filho, Petronio Filgueiras,Miller, Joseph,Simas, Alfredo Mayall,Lira, Bruno Freitas,De Souza Luis, José Alixandre,Zuckerman-Schpector, Júlio

, p. 685 - 690 (2007/10/03)

Mesoionic 2,4-diphenyl-3-methyl-1,3-thiazolium-5-thiolate, 2-(4′-chlorophenyl)-3-methyl-4-phenyl-1,3-thiazolium-5-thiolate and 2-(4′-chlorophenyl)-3-methyl-4-(4′-isopropyl-phenyl)-1,3- thiazolium-5-thiolate were synthesized via N-methyl-C-aryl-glycines, i

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