Basic information Safety Supplier Related

2-(2-Hydroxyphenyl)benzothiazole

Basic information Safety Supplier Related

2-(2-Hydroxyphenyl)benzothiazole Basic information

Product Name:
2-(2-Hydroxyphenyl)benzothiazole
Synonyms:
  • 2-(2-BENZOTHIAZOLYL)PHENOL
  • 2-(2-HYDROXYPHENYL)BENZOTHIAZOLE
  • 2-(BENZO[D]THIAZOL-2-YL)PHENOL
  • 2-(O-HYDROXYPHENYL)BENZOTHIAZOLE
  • TIMTEC-BB SBB005787
  • O-(2-BENZOTHIAZOLYL)PHENOL
  • 2-(1,3-Benzothiazol-2-yl)phenol
  • 2-(2-benzothiazolyl)-pheno
CAS:
3411-95-8
MF:
C13H9NOS
MW:
227.28
EINECS:
222-299-9
Product Categories:
  • Fluorescent
  • Building Blocks
  • Heterocyclic Building Blocks
  • Thiazoles
Mol File:
3411-95-8.mol
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2-(2-Hydroxyphenyl)benzothiazole Chemical Properties

Melting point:
128-132 °C (lit.)
Boiling point:
175-193 °C
Density 
1.2168 (rough estimate)
refractive index 
1.6800 (estimate)
storage temp. 
under inert gas (nitrogen or Argon) at 2-8°C
solubility 
Solubility Insoluble in water; soluble in ethanol
form 
Solid
pka
8.21(at 25℃)
color 
White to Light yellow
PH Range
Non0 uorescence (<9.3) to blue-green 0 uorescence (9.3)
BRN 
173026
Major Application
Organic light emitting devices, electroluminescent devices, laser dyes, photography, plastic scintillation applications, herbicides, eyeglass lenses, cosmetics
CAS DataBase Reference
3411-95-8(CAS DataBase Reference)
NIST Chemistry Reference
Phenol, o-(2-benzothiazolyl)-(3411-95-8)
EPA Substance Registry System
Phenol, 2-(2-benzothiazolyl)- (3411-95-8)
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-37/39-24/25
WGK Germany 
3
RTECS 
SJ7360000
Hazard Note 
Irritant
TSCA 
Yes
HS Code 
29342000

MSDS

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2-(2-Hydroxyphenyl)benzothiazole Usage And Synthesis

Chemical Properties

Off-white to yellow powder

Definition

ChEBI: 2-(1,3-benzothiazol-2-yl)phenol is a member of the class of benzothiazoles that is 1,3-benzothiazole substituted by a 2-hydroxyphenyl group at position 2. It has a role as a geroprotector. It is a member of phenols and a member of benzothiazoles.

Purification Methods

Recrystallise it several times from aqueous EtOH or dilute AcOH and sublime it. [Itoh & Fujiwara J Am Chem Soc 107 1561 1985, Bogert & Corbitt J Am Chem Soc 48 786 1926, Beilstein 27 II 91.]

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