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5-Methylthiazole-2(3H)-thione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 17626-82-3 Structure
  • Basic information

    1. Product Name: 5-Methylthiazole-2(3H)-thione
    2. Synonyms: 5-Methylthiazole-2(3H)-thione
    3. CAS NO:17626-82-3
    4. Molecular Formula: C4H5NS2
    5. Molecular Weight: 131.22
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 17626-82-3.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: 5-Methylthiazole-2(3H)-thione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5-Methylthiazole-2(3H)-thione(17626-82-3)
    11. EPA Substance Registry System: 5-Methylthiazole-2(3H)-thione(17626-82-3)
  • 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: 17626-82-3(Hazardous Substances Data)

17626-82-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 17626-82-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,7,6,2 and 6 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 17626-82:
(7*1)+(6*7)+(5*6)+(4*2)+(3*6)+(2*8)+(1*2)=123
123 % 10 = 3
So 17626-82-3 is a valid CAS Registry Number.

17626-82-3SDS

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 5-Methyl-1,3-thiazol-2(3H)-thion

1.2 Other means of identification

Product number -
Other names 5-methyl-3H-thiazole-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:17626-82-3 SDS

17626-82-3Relevant articles and documents

Substituted heterocyclic analogs as selective COX-2 inhibitors in the flosulide class

Ouimet, Nathalie,Chan, Chi-Chung,Charleson, Stella,Claveau, David,Gordon, Robert,Guay, Daniel,Chun-Sing, Li,Ouellet, Marc,Percival, David M.,Riendeau, Denis,Wong, Elizabeth,Zamboni, Robert,Prasit, Petpiboon

, p. 151 - 156 (1999)

Substituted heterocyclic analogs in the Flosulide class were investigated as potential selective cyclooxygenase-2 inhibitors. 6-(4-Ethyl- 2-thiazolylthio)-5-methanesulfonamido-3H-isobenzofuran-1-one 14 was found to be the optimal compound in the series wi

CARBACEPHEM BETA-LACTAM ANTIBIOTICS

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Page/Page column 62, (2010/11/05)

Carbacephem β-lactam antibiotics having chemical structures (I) and (II) are disclosed: including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar2, R1, R2 and R6 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.

CARBACEPHEM β-LACTAM ANTIBIOTICS

-

Page/Page column 88, (2010/04/06)

Carbacephem -lactam antibiotics having structure (I) are disclosed, including stereoisomers, pharmaceutically acceptable salts, esters and prodrugs thereof, wherein Ar1, Ar2, R1 and R2 are as defined herein. The compounds are useful for the treatment of bacterial infections, in particular those caused by methicillin-resistant Staphylococcus spp.

Rearrangement reactions; 14: Synthesis of functionalized thiazoles via attack of heteroatom nucleophiles on allenyl isothiocyanates

Banert, Klaus,Al-Hourani, Baker Jawabrah,Groth, Stefan,Vrobel, Kai

, p. 2920 - 2926 (2007/10/03)

Treatment of allenyl isothiocyanates with sulfur-, oxygen-, nitrogen- or hydride-containing nucleophiles such as propane-2-thiol, thiophenol, hydrogen sulfide, alcohols, phenol or aqueous NaOH, NH3, primary or secondary aliphatic or aromatic amines, N,N,N′,N′-tetramethylguanidine or sodium cyanoborohydride resulted in ring closure to generate thiazoles bearing a functionality at position C-2 in most cases. Moreover, we report the first examples of aromatic miazole-2-phosphonates prepared by the same strategy using dialkyl or diphenyl phosphites as nucleophiles. Georg Thieme Verlag Stuttgart.

SYNTHESIS AND REACTIONS OF NEW VINYL ISOTHIOCYANATES

Banert, Klaus,Groth, Stefan,Hueckstaedt, Holger,Vrobel, Kai

, p. 323 - 324 (2007/10/02)

New vinyl isothiocyanates, which can be prepared from easily accessible thiocyanates by sigmatropic shifts, show unusually high reactivity used for the synthesis of heterocyclic sulfur compounds.

Alkylation, Acylation, and Carbamoylation Products of 5-Methylene-1,3-thiazolidine-2-thione

Hanefeld, Wolfgang,Bercin, Erdogan

, p. 58 - 64 (2007/10/02)

The reaction product of prop-2-inylamine and carbon disulfide was contrary to earlier results identified as 5-methylene-1,3-thiazolidine-2-thione (3a).This was reacted with alkyl halides, acyl, carbamoyl, and thiocarbamoyl chlorides.The structures of the

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