2-Methyinaphtho[1,2-d]thiazole
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
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)
Safety Information
- Safety Statements
- 22-24/25
- WGK Germany
- 3
- TSCA
- Yes
- HS Code
- 29349990
MSDS
- Language:English Provider:2-Methyinaphtho[1,2-d]thiazole
- Language:English Provider:SigmaAldrich
- Language:English Provider:ACROS
- Language:English Provider:ALFA
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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