Basic information Safety Supplier Related

2-(METHYLTHIO)-2-THIAZOLINE

Basic information Safety Supplier Related

2-(METHYLTHIO)-2-THIAZOLINE Basic information

Product Name:
2-(METHYLTHIO)-2-THIAZOLINE
Synonyms:
  • 2-methylsulfanyl-4,5-dihydrothiazoline
  • 2-Methylsulfanyl-4,5-dihydro-thiazole
  • 2-(Methylsulfanyl)-4,5-dihydro-1,3-thiazole
  • 2-(Methylthio)thiazoline
  • 2-Thiazoline, 2-(methylthio)-
  • 2-(METHYLMERCAPTO)-2-THIAZOLINE
  • 2-(METHYLTHIO)-2-THIAZOLINE
  • 2-(Methylthio)-4,5-dihydro-1,3-thiazole
CAS:
19975-56-5
MF:
C4H7NS2
MW:
133.24
EINECS:
243-447-9
Product Categories:
  • chemical additive
  • pharmaceutical intermediate
  • Building Blocks
  • Chemical Synthesis
  • Heterocyclic Building Blocks
  • Thiazolines/Thiazolidines
Mol File:
19975-56-5.mol
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2-(METHYLTHIO)-2-THIAZOLINE Chemical Properties

Boiling point:
216-217 °C (lit.)
Density 
1.226 g/mL at 25 °C (lit.)
refractive index 
n20/D 1.592(lit.)
Flash point:
208 °F
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
clear liquid
pka
4.74±0.10(Predicted)
color 
Colorless to Light yellow
BRN 
106353
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Safety Information

Safety Statements 
23-24/25
RIDADR 
UN 3334
WGK Germany 
3
8-9-13
HS Code 
29341000

MSDS

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2-(METHYLTHIO)-2-THIAZOLINE Usage And Synthesis

Uses

thiazolidin e thione pharmaceutical intermediate

Uses

2-(Methylthio)-2-thiazoline has been used in the preparation of:

  • novel tri- and tetracyclic hetero systems, via reaction with heteroaromatic 2-aminoesters
  • 2-(2-chlorobenzylamino)-2-thiazoline

Synthesis

134469-06-0

74-88-4

19975-56-5

General procedure for the synthesis of 2-methylthio-2-thiazoline from thiazolidine-2-thione and iodomethane: Thiazolidine-2-thione (2 g, 0.0168 mol) was dissolved in acetonitrile (20 ml) and iodomethane (1.04 ml, 0.0168 mol) was added. The reaction mixture was heated to reflux for 3 hours and subsequently cooled to room temperature. The reaction mixture was filtered and the white solid obtained was collected. The solid was poured into saturated potassium carbonate solution (20 ml) to form an oil. The oily substance was extracted with dichloromethane and the organic phase was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give a colorless liquid product (1.4 g, 63% yield).

References

[1] Synthetic Communications, 2006, vol. 36, # 22, p. 3339 - 3343
[2] Patent: CN105481846, 2016, A. Location in patent: Paragraph 0006; 0007
[3] Journal of the American Chemical Society, 1958, vol. 80, p. 3335,3338
[4] Journal of Organic Chemistry, 1961, vol. 26, p. 85 - 88
[5] Helvetica Chimica Acta, 1978, vol. 61, p. 3143 - 3148

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