Basic information Safety Supplier Related

2-Methyinaphtho[1,2-d]thiazole

Basic information Safety Supplier Related

2-Methyinaphtho[1,2-d]thiazole Basic information

Product Name:
2-Methyinaphtho[1,2-d]thiazole
Synonyms:
  • 2-d]thiazole,2-methyl-naphtho[
  • 2-d]thiazole,2-methyl-Naphtho[1
  • Naphth[1,2-d]thiazole, 2-methyl-
  • AURORA KA-80
  • 2-METHYLNAPHTHOL[1,2-D]THIAZOLE
  • 2-METHYLNAPHTHO[1,2-D]THIAZOLE
  • 2-METHYLNAPHTHO[1,2-D][1,3]THIAZOLE
  • 2-METHYL-BETA-NAPHTHYLTHIAZOLE
CAS:
2682-45-3
MF:
C12H9NS
MW:
199.27
EINECS:
220-240-1
Product Categories:
  • Thiazoles
  • Intermediates of Dyes and Pigments
  • BENZOTHIAZOLE
  • Building Blocks
  • C12 to C20+
  • Chemical Synthesis
  • Heterocyclic Building Blocks
Mol File:
2682-45-3.mol
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2-Methyinaphtho[1,2-d]thiazole Chemical Properties

Melting point:
95-97 °C(lit.)
Boiling point:
168 °C / 5.5mmHg
Density 
1.1171 (rough estimate)
refractive index 
1.5500 (estimate)
storage temp. 
Keep in dark place,Sealed in dry,Room Temperature
form 
powder to crystal
pka
1.65±0.30(Predicted)
color 
White to Light yellow
CAS DataBase Reference
2682-45-3(CAS DataBase Reference)
NIST Chemistry Reference
Naphtho[1,2-d]thiazole, 2-methyl-(2682-45-3)
EPA Substance Registry System
Naphtho[1,2-d]thiazole, 2-methyl- (2682-45-3)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
TSCA 
Yes
HS Code 
29349990

MSDS

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2-Methyinaphtho[1,2-d]thiazole Usage And Synthesis

Chemical Properties

light yellow to beige-brown crystalline powder

Synthesis

63512-54-9

108-24-7

2682-45-3

1. 1-Aminonaphthalene-2-thiol and 20 mg of sodium dodecyl sulfate were added to 20 mL of water and stirred until a homogeneous mixture was formed. 2. 7.5 mmol of ethanoic anhydride was slowly added to the mixture and stirring was continued for 5 minutes. 3. A precipitate was produced from the reaction mixture over a period of 5-10 minutes. 4. The precipitate was collected by filtration, washed twice with 1 mL of water, and subsequently dried under vacuum. 5. The un-precipitated reaction mixture was extracted twice with 25 mL of ethyl acetate. 6. Ethyl acetate was used to extract the unprecipitated reaction mixture twice.6. The organic layers were combined and dried over anhydrous sodium sulfate.7. The solvent was removed under reduced pressure using a rotary evaporator to give 2-methyl-β-naphthothiazole in 70% yield.

References

[1] Patent: WO2007/78184, 2007, A1. Location in patent: Page/Page column 14-15
[2] Patent: US2008/200678, 2008, A1. Location in patent: Page/Page column 6

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