Basic information Safety Supplier Related

4-Benzothiazolol

Basic information Safety Supplier Related

4-Benzothiazolol Basic information

Product Name:
4-Benzothiazolol
Synonyms:
  • 4-Benzothiazolol
  • Benzothiazol-4-ol
  • 4-Benzothiazolol(6CI,8CI,9CI)
  • 4-hydroxybenzothiazole
  • benzo[d]thiazol-4-ol
  • 4-Benzothiazolol(saMeasBTA-4-0651)
  • 1,3-benzothiazol-4-ol
  • 4-hydroxy-benzothiazol
CAS:
7405-23-4
MF:
C7H5NOS
MW:
151.19
Product Categories:
  • BENZOTHIAZOLE
Mol File:
7405-23-4.mol
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4-Benzothiazolol Chemical Properties

Melting point:
143℃
Boiling point:
312℃
Density 
1.444
Flash point:
142℃
storage temp. 
Sealed in dry,Room Temperature
form 
solid
pka
7.71±0.40(Predicted)
color 
Light green to green
InChI
InChI=1S/C7H5NOS/c9-5-2-1-3-6-7(5)8-4-10-6/h1-4,9H
InChIKey
NZFKDDMHHUEVPI-UHFFFAOYSA-N
SMILES
S1C2=CC=CC(O)=C2N=C1
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Safety Information

HS Code 
2934208090
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4-Benzothiazolol Usage And Synthesis

Uses

Benzo[d]thiazol-4-ol is a constituent of pheomelanin; a polymeric skin-?centered pigment which acts as a natural photoprotector against harmful solar-?UV radiation.

Synthesis

3048-46-2

7405-23-4

General procedure for the synthesis of 4-hydroxybenzothiazole from 4-methoxybenzothiazole: Boron bromide (3.09 mL, 1M DCM solution, 3.09 mmol) was slowly added dropwise to a stirring solution of 4-methoxybenzothiazole (510 mg, 3.09 mmol) in anhydrous dichloromethane (30 mL) at 0 °C. The reaction mixture was gradually warmed to 40 °C and stirred continuously overnight. Upon completion of the reaction, the solution was concentrated under vacuum and subsequently diluted with water and 2N hydrochloric acid. The aqueous phase was neutralized to pH 7 with sodium bicarbonate and then extracted with ethyl acetate (3 x 100 mL). The organic extracts were combined, dried with magnesium sulfate, and the solvent was removed under vacuum. The resulting oil was purified by fast chromatography on a silica gel column with the eluent ratio tapered from hexane:ethyl acetate [4:1] to hexane:ethyl acetate [7:3], resulting in 4-hydroxybenzothiazole as a brown solid (730 mg, 80% yield). The NMR hydrogen spectrum (300 MHz, CDCl3) data were as follows: δ 7.59 (1H, s, hydrogen on the thiazole ring), 7.46 (1H, dd, aromatic hydrogen), 7.36 (1H, t, aromatic hydrogen), 7.02 (1H, dd, aromatic hydrogen).

References

[1] Patent: WO2004/43903, 2004, A1. Location in patent: Page 68 - 69
[2] Patent: WO2004/43904, 2004, A1. Location in patent: Page 64 - 65
[3] Patent: WO2004/43931, 2004, A1. Location in patent: Page 42-43
[4] Bioorganic and Medicinal Chemistry Letters, 2010, vol. 20, # 21, p. 6199 - 6202
[5] Helvetica Chimica Acta, 1938, vol. 21, p. 709

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