112143
2-Methylbenzothiazole
99%
Synonym(s):
2-Methyl-1,3-benzothiazole, 2-Methylbenzo[d]thiazole
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About This Item
Empirical Formula (Hill Notation):
C8H7NS
CAS Number:
Molecular Weight:
149.21
Beilstein/REAXYS Number:
112427
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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assay
99%
refractive index
n20/D 1.617 (lit.)
bp
238 °C (lit.)
mp
11-14 °C (lit.)
density
1.173 g/mL at 25 °C (lit.)
SMILES string
Cc1nc2ccccc2s1
InChI
1S/C8H7NS/c1-6-9-7-4-2-3-5-8(7)10-6/h2-5H,1H3
InChI key
DXYYSGDWQCSKKO-UHFFFAOYSA-N
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General description
2-Methylbenzothiazole can be synthesized by the Cu-catalyzed, base-free C-S coupling using conventional and microwave heating methods.
Application
Reagent employed in the synthesis of polycarbocyanine and thiacyanine dyes, as well as (arylfuryl)benzothiazoles.
Storage Class
10 - Combustible liquids
wgk_germany
WGK 3
flash_point_f
215.6 °F - closed cup
flash_point_c
102 °C - closed cup
ppe
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
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S-aryl thioacetates can be prepared by reaction of inexpensive potassium thioacetate with both electron-rich and electron-poor aryl iodides under a base-free copper/ligand catalytic system. CuI as copper source affords S-aryl thioacetates in good to excellent yields, by using 1,10-phenanthroline as
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