2-(2-Hydroxyphenyl)benzothiazole supplier

Name
2-(2-Hydroxyphenyl)benzothiazole
EINECS 222-299-9
CAS No. 3411-95-8
Article Data178
CAS DataBase
Density 1.337 g/cm³
Solubility
Melting Point 128-132 °C(lit.)
Formula C₁₃H₉NOS
Boiling Point 402.184 °C at 760 mmHg
Molecular Weight 227.287
Flash Point 197.034 °C
Transport Information
Appearance Off-white to yellow powder
Safety 26-37/39
Risk Codes 36/37/38
Molecular Structure
Hazard Symbols Xi
Synonyms Phenol,o-2-benzothiazolyl- (6CI,7CI,8CI);2-(2-Benzothiazolyl)phenol;2-(2'-Hydroxyphenyl)-2-benzothiazole;2-(2'-Hydroxyphenyl)benzothiazole;2-(Benzo[d]thiazol-2-yl)phenol;2-(o-Hydroxyphenyl)benzothiazole;HBT;NSC 5051;NSC 58548;
PSA 61.36000
LogP 3.66890

Synthetic route

: 90-02-8
salicylaldehyde

: 137-07-5
2-amino-benzenethiol

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With cadmium sulphide In methanol at 20℃; for 0.333333h; Catalytic behavior; Irradiation;	98%
With 3,6-di(2'-pyridyl)-1,2,4,5-tetrazine In ethanol at 20℃; for 0.5h; Irradiation; Green chemistry;	98%
With manganese doped CdS nanoparticles In water at 90℃; for 1.5h; chemoselective reaction;	98%

: 89-95-2
2-methyl-benzyl alcohol

: 137-07-5
2-amino-benzenethiol

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With 1-pentyl-3-methylimidazolium bromide for 0.0583333h; microwave irradiation;	95%
With iodine In N,N-dimethyl-formamide at 100℃; for 0.5h;	81%
With iodine at 20℃; for 0.25h;	80%
With zirconium(IV) oxychloride for 0.0666667h; Irradiation; microwave;	76%
With silica gel for 0.0833333h; microwave irradiation;	87 % Chromat.

: 137-07-5
2-amino-benzenethiol

: 69-72-7
salicylic acid

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
Stage #1: 2-amino-benzenethiol; salicylic acid In toluene at 80℃; for 1h; Stage #2: With phosphorus trichloride In toluene at 40 - 100℃; for 6h;	92%
Stage #1: 2-amino-benzenethiol; salicylic acid In toluene at 100℃; for 1h; Stage #2: With phosphorus trichloride In toluene at 40 - 60℃; for 6.5h;	92%
With polyphosphoric acid at 180℃; for 3h;	85%

: 90-02-8
salicylaldehyde

: 1141-88-4
2-Aminophenyl disulfide

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With oxygen In water for 4h; Catalytic behavior; Reflux; Green chemistry;	91%
With toluene-4-sulfonic acid In PEG-200/400 for 0.166667h; Microwave irradiation;	89%
In glycerol at 175℃; for 0.75h; Green chemistry;	81.1%

: 7361-94-6
2-(2-hydroxyphenyl)benzothiazoline

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With sodium hypochlorite In ethanol at 20℃; for 1h;	90%
With Dowex 50W In water at 90℃; for 25h;	70%
With (2,3,4,5,6-pentafluorophenyl)ammonium triflate; oxygen In water for 10h; Reflux;	70%
With sodium cyanide In N,N-dimethyl-formamide	810 mg
for 10h; UV-irradiation;

: 615-43-0
2-iodophenylamine

: 90-02-8
salicylaldehyde

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With 1,10-Phenanthroline; copper(II) choride dihydrate; potassium carbonate; sulfur In water at 100℃; for 24h;	90%

: 74405-07-5
4-chloro-2,2-dimethyl-2H-benzo[e][1,3]oxazine

: 137-07-5
2-amino-benzenethiol

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
In acetonitrile for 1h; Heating;	89%

: 444-30-4
2-(trifluoromethyl)phenol

: 137-07-5
2-amino-benzenethiol

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With sodium hydroxide In water at 80℃; for 2h;	88%
With sodium hydroxide at 90℃; for 1h; Inert atmosphere;	86%
With sodium hydroxide at 90℃; for 1h; Inert atmosphere; Schlenk technique;	80%
With sodium hydroxide

: 1039984-47-8
2-hydroxy-N-(2-iodophenyl)benzamide

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
Stage #1: 2-hydroxy-N-(2-iodophenyl)benzamide With copper(l) iodide; sodiumsulfide nonahydrate In N,N-dimethyl-formamide at 80℃; for 12h; Stage #2: With hydrogenchloride In N,N-dimethyl-formamide at 20℃;	85%

: 95-16-9
1,3-Benzothiazole

: 5661-50-7
N-(phenoxy)acetamide

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; cesium acetate; silver(I) triflimide In dimethyl sulfoxide at 85℃; for 30h; Inert atmosphere;	85%

: 1354644-30-6
N-(2-allyloxybenzylidene)-2-phenylthiobenzenamine

A: 92-52-4
biphenyl

B: 3411-95-8
2-(benzothiazol-2-yl)phenol

C: 1745-81-9
2-Allylphenol

Conditions

Conditions	Yield
at 150 - 650℃; under 0.013 Torr; for 0.25h; Pyrolysis;	A 2% B 84% C 9%

...Expand

: 883-93-2
2-Phenylbenzothiazole

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With sodium persulfate; palladium diacetate In 1,4-dioxane at 80℃; for 12h; Reagent/catalyst; Inert atmosphere;	83%
With Bromotrichloromethane; (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile; oxygen; palladium diacetate In cyclohexane; 1,2-dichloro-ethane at 20℃; for 24h; Solvent; Irradiation;	61%
With [bis(acetoxy)iodo]benzene; palladium diacetate; trifluoroacetic acid at 110℃; for 6h; Catalytic behavior; Reagent/catalyst; Solvent; Time; Concentration; regioselective reaction;

: 883-93-2
2-Phenylbenzothiazole

: 64-19-7
acetic acid

A: 3411-95-8
2-(benzothiazol-2-yl)phenol

B: 1422963-57-2
2-(benzo[d]thiazol-2-yl)-3-hydroxyphenyl acetate

Conditions

Conditions	Yield
With [bis(acetoxy)iodo]benzene; palladium diacetate at 110℃; for 5h; Catalytic behavior; Concentration; Reagent/catalyst; Time; Overall yield = 90 %; regioselective reaction;	A 81% B 9%

...Expand

: C16H11NO4S

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With sodium phosphate In dimethyl sulfoxide at 20℃; for 24h;	81%

: 4-(2-benzothiazol-2-yl-phenoxymethyl)-benzoic acid methyl ester

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With magnesium In tetrahydrofuran; methanol at 20℃; for 10h;	77%

: 883-93-2
2-Phenylbenzothiazole

: 64-19-7
acetic acid

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile; oxygen; palladium diacetate; potassium trifluoroacetate In N,N-dimethyl-formamide at 70℃; for 24h; Catalytic behavior; Reagent/catalyst; Solvent; Temperature; Irradiation;	75%

: 17392-16-4
(2-hydroxyphenyl)oxoacetic acid

: 137-07-5
2-amino-benzenethiol

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With dihydrogen peroxide In 1,4-dioxane; water at 20℃; for 8h; Irradiation;	73%

: 95-16-9
1,3-Benzothiazole

: 90-02-8
salicylaldehyde

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With tert.-butylhydroperoxide; N-chloro-succinimide In decane; dimethyl sulfoxide at 120℃; for 12h; Inert atmosphere;	71%
With tert.-butylhydroperoxide; N-chloro-succinimide In decane; dimethyl sulfoxide at 120℃; for 10h; Schlenk technique;	71%
With di-tert-butyl peroxide In 1-methyl-pyrrolidin-2-one at 100℃; for 3h;	47%

: 69-72-7
salicylic acid

: 1141-88-4
2-Aminophenyl disulfide

A: 3411-95-8
2-(benzothiazol-2-yl)phenol

B: C20H15NO4S

Conditions

Conditions	Yield
Stage #1: salicylic acid; 2-Aminophenyl disulfide In toluene at 70℃; for 2.5h; Inert atmosphere; Stage #2: With phosphorus trichloride In toluene at 30 - 100℃; Inert atmosphere;	A 66% B n/a

...Expand

: 90-02-8
salicylaldehyde

: 105-56-6
ethyl 2-cyanoacetate

: 137-07-5
2-amino-benzenethiol

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
In butan-1-ol for 7h; Reflux;	65%
With benzoic acid In butan-1-ol at 110℃; for 8h;	62%

...Expand

: 90-02-8
salicylaldehyde

: 88-73-3
2-Chloronitrobenzene

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With 4-methyl-morpholine; sulfur at 130℃; for 16h; Sealed tube; Inert atmosphere;	62%

: 58402-38-3
2-hydroxybenzyl bromide

: 137-07-5
2-amino-benzenethiol

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
In acetonitrile Irradiation; chemoselective reaction;	61%

: C20H13NO2S2

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With gold(III) chloride In methanol; water	57%

: 95-16-9
1,3-Benzothiazole

: 533-58-4
2-Iodophenol

A: 4-(2-hydroxyphenyl)-4,7-dihydrobenzothiazole

B: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With 2,2'-azobis(isobutyronitrile); diphenyl diselenide; tri-n-butyl-tin hydride In benzene for 1h; Heating;	A 7% B 19%

...Expand

: 87-17-2
salicylanilide

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With sulfur

: 3292-42-0
2-aminobenzenethiol hydrochloride

: 90-02-8
salicylaldehyde

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With ethanol

: 137-07-5
2-amino-benzenethiol

: 65-45-2
salicylamide

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
at 240 - 250℃;

: 27655-26-1
benzothiazole 3-oxide

: 1608-42-0
benzenedizolium-2-carboxylate

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
In tert-butyl alcohol

: 779-84-0
N-phenylsalicylaldimine

: 3411-95-8
2-(benzothiazol-2-yl)phenol

Conditions

Conditions	Yield
With sulfur Heating;

: scandium isopropoxide

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 1190879-78-7
Sc(III)-tris-2-(2-benzthiazol-2-yl)phenolate

Conditions

Conditions	Yield
In acetonitrile at 20℃; Inert atmosphere; Reflux;	100%

: beryllium sulfate

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 236753-06-3
Be(2-(2'-oxyphenyl)benzothiazole)2]

Conditions

Conditions	Yield
With sodium hydroxide In methanol at 20℃; Inert atmosphere;	100%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 22883-70-1
(4-hydroxy-phenyl)triphenylphosphonium bromide

: C24H20OP(1+)*C13H8NOS(1-)

Conditions

Conditions	Yield
Stage #1: 2-(benzothiazol-2-yl)phenol With sodium methylate In methanol at 20℃; for 2h; Stage #2: (4-hydroxy-phenyl)triphenylphosphonium bromide In methanol at 20℃; for 2h;	99%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 13499-05-3
hafnium tetrachloride

: 1210945-34-8
tetrakis(2-(2-hydroxyphenyl)benzothiazole)hafnium

Conditions

Conditions	Yield
With piperidine In ethanol at 20℃; Inert atmosphere; Reflux;	98%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 31643-49-9
4-Nitrophthalonitrile

: 1578263-21-4
4-(2-(benzo[d]thiazol-2-yl)phenoxy)phthalonitrile

Conditions

Conditions	Yield
Stage #1: 2-(benzothiazol-2-yl)phenol; 4-Nitrophthalonitrile In N,N-dimethyl-formamide at 50℃; for 0.166667h; Inert atmosphere; Stage #2: With potassium carbonate In N,N-dimethyl-formamide at 50℃; for 122h; Inert atmosphere;	97%

: bis(tert-butylimido)bis(tert-butylamido)tungsten

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: bis(tert-butylimido)bis(2-benzothiazolyl-2-phenolato)tungsten

Conditions

Conditions	Yield
In toluene chelate ligand is added to soln. of the W compd. in toluene under argon, soln. is refluxed for 2 min, cooled to room temp.; concd. (vac.), addn. of hexane, cooling to -20°C, filtn., washing (hexane), drying (vac.); elem. anal.;	96%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 106-95-6
allyl bromide

: 2-(2-(allyloxy)phenyl)benzo[d]thiazole

Conditions

Conditions	Yield
With potassium carbonate In acetone for 2h; Reflux;	96%
With potassium carbonate In tetrahydrofuran for 3h; Reflux;	50%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: bis(μ-hydroxo)bis(tris(3,5-dimethylpyrazolyl)borate)dinickel(II)

: 1610351-76-2
[Ni(hydrotris(3,5-dimethylpyrazolyl)borate)(2-(2'-hydroxylphenyl)benzothiazole(-1H))]

Conditions

Conditions	Yield
In chloroform	94%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: tris(bistrimethylsilylamine)scandium(III)

: 1190879-78-7
Sc(III)-tris-2-(2-benzthiazol-2-yl)phenolate

Conditions

Conditions	Yield
In 1,2-dimethoxyethane soln. of benzothiazole in DME was added to soln. of scandium complex in DME, stirred for 30 min at room temp.; evapd. in vac., washed with toluene, dried in vac., elem. anal.;	93%

: tris(bis(trimethylsilyl)amido)samarium(III)

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 1422197-95-2
tetra(2-(2-hydroxyphenyl)-benzothiazolato)di(μ-2-(2-hydroxyphenyl)benzothiazolato)Sm2

Conditions

Conditions	Yield
In Dimethyl ether at 20℃; for 0.5h;	93%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: diphenylborinic anhydride

: 2-(2-((diphenylboryl)oxy)phenyl)benzo[d]thiazole

Conditions

Conditions	Yield
In tetrahydrofuran for 2h; Inert atmosphere; Reflux;	92%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 16-oxo-1-oxa-4-azacyclohexadecane-4-carbonyl chloride

: 2-(benzo[d]thiazol-2-yl)phenyl 16-oxo-1-oxa-4-azacyclohexadecane-4-carboxylate

Conditions

Conditions	Yield
With dmap; triethylamine In dichloromethane at 20℃; Cooling with ice;	92%

: tris[N,N-bis(trimethylsilyl)amide]gadolinium(III)

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 1422198-04-6
tetra(2-(2-hydroxyphenyl)-benzothiazolato)di(μ-2-(2-hydroxyphenyl)benzothiazolato)Gd2

Conditions

Conditions	Yield
In Dimethyl ether at 20℃; for 0.5h;	91%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 43185-52-0
ethoxydiphenylborane

: 2-(2-((diphenylboryl)oxy)phenyl)benzo[d]thiazole

Conditions

Conditions	Yield
In ethanol at 50℃; for 3h; Inert atmosphere;	91%

: 14853-14-6
tetraphenylarsonium tetrachlorooxorhenate(V)

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 116887-58-2
As(C6H5)4{ReOCl3(hbt)}

Conditions

Conditions	Yield
In isopropyl alcohol mixing of a 2-fold molar excess of 2-(2-hydroxyphenyl)benzothiazole with a soln. of As(C6H5)4(ReOCl4) in isopropanol (25°C) to form immediately a ppt.; filtration, washing (isopropanol, diethyl ether), recrystn. (CH2Cl2, ethanol); elem. anal.;	90%

: 116887-56-0
{As(C6H5)4}(1+)*{(99)TcOBr4}(1-)={As(C6H5)4}{(99)TcOBr4}

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 116887-54-8
As(C6H5)4{TcOBr3(hbt)}

Conditions

Conditions	Yield
In isopropyl alcohol mixing of a 2-fold molar excess of 2-(2-hydroxyphenyl)benzothiazole with a soln. of As(C6H5)4(TcOBr4) in isopropanol (25°C) to form immediately a ppt.; filtration, washing (isopropanol, diethyl ether), recrystn. (CH2Cl2, ethanol); elem. anal.;	90%

: 14853-12-4
{As(C6H5)4}(1+)*{ReOBr4}(1-)={As(C6H5)4}{ReOBr4}

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 116887-60-6
As(C6H5)4{ReOBr3(hbt)}

Conditions

Conditions	Yield
In isopropyl alcohol mixing of a 2-fold molar excess of 2-(2-hydroxyphenyl)benzothiazole with a soln. of As(C6H5)4(ReOBr4) in isopropanol (25°C) to form immediately a ppt.; filtration, washing (isopropanol, diethyl ether), recrystn. (CH2Cl2, ethanol); elem. anal.;	90%

: 97101-52-5
As(C6H5)4(1+)*(99)Tc(O)Cl4(1-) = [As(C6H5)4][(99)Tc(O)Cl4]

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 116887-52-6
tetraphenylarsonium oxotrichloro{2-(2-hydroxyphenyl)benzothiazolato}technetate(V)

Conditions

Conditions	Yield
In isopropyl alcohol mixing of a 2-fold molar excess of 2-(2-hydroxyphenyl)benzothiazole with a soln. of As(C6H5)4(TcOCl4) in isopropanol (25°C) to form immediately a ppt.; filtration, washing (isopropanol, diethyl ether), recrystn. (CH2Cl2, ethanol); elem. anal.;	90%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 279216-12-5
1-(6-(chloromethyl)pyridine-2-yl)-N,N-bis(pyridine-2-ylmethyl)methaneamine

: 1414968-71-0
C32H27N5OS

Conditions

Conditions	Yield
With potassium carbonate In N,N-dimethyl-formamide at 90℃;	90%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 76-05-1
trifluoroacetic acid

: 1428114-89-9
5-(benzo[d]thiazol-2-yl)-4-hydroxyisophthalaldehyde

Conditions

Conditions	Yield
With hexamethylenetetramine Reflux;	90%
With hexamethylenetetramine for 0.166667h; Reflux;	90%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 2937-50-0
Allyl chloroformate

: allyl (2-(benzo[d]thiazol-2-yl)phenyl) carbonate

Conditions

Conditions	Yield
With triethylamine In tetrahydrofuran at 0 - 20℃; for 2.5h;	90%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 79-04-9
chloroacetyl chloride

: chloro-acetic acid 2-benzothiazol-2-yl-phenyl ester

Conditions

Conditions	Yield
Stage #1: 2-(benzothiazol-2-yl)phenol With potassium carbonate In tetrahydrofuran for 0.5h; Stage #2: chloroacetyl chloride In tetrahydrofuran at 20 - 50℃; for 12h; Reagent/catalyst; Solvent; Temperature;	90%

: 3411-95-8
2-(benzothiazol-2-yl)phenol

: 12-oxo-1-oxa-4-azacyclododecane-4-carbonyl chloride

: 2-(benzo[d]thiazol-2-yl)phenyl 12-oxo-1-oxa-4-azacyclododecane-4-carboxylate

Conditions

Conditions	Yield
With dmap; triethylamine In dichloromethane at 20℃; Cooling with ice;	90%

2-(2-Hydroxyphenyl)benzothiazole Chemical Properties

IUPAC Name: 6-(3H-1,3-benzothiazol-2-ylidene)cyclohexa-2,4-dien-1-one
The MF of 2-(2-Hydroxyphenyl)benzothiazole(3411-95-8): C₁₃H₉NOS
The MW of 2-(2-Hydroxyphenyl)benzothiazole(3411-95-8): 227.28
EINECS: 222-299-9
mp: 128-132 °C(lit.)
Density: 1.365 g/cm³
Flash Point: 190.8 °C
Boiling Point: 391.8 °C at 760 mmHg
Index of Refraction: 1.714
Appearance: Off-white crystals.
Solubility in water: Insoluble
Categories: Building Blocks;Heterocyclic Building Blocks;Thiazoles
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
The Structure of 2-(2-Hydroxyphenyl)benzothiazole(3411-95-8):

2-(2-Hydroxyphenyl)benzothiazole Safety Profile

Hazard Codes:

Xi
Risk Statements: 36/37/38
36/37/38: Irritating to eyes, respiratory system and skin
Safety Statements: 26-37/39
26: In case of contact with eyes, rinse immediately with plenty of water and seek medical advice
37/39: Wear suitable gloves and eye/face protection
WGK Germany: 3
RTECS: SJ7360000
Hazard Note: Irritant

2-(2-Hydroxyphenyl)benzothiazole Specification

1. First Aid Measures
Ingestion:
If victim is conscious and alert, give 2-4 cupfuls of milk or water. Never give anything by mouth to an unconscious person. Get medical aid immediately.
Inhalation:
Remove from exposure to fresh air immediately. If not breathing, give artificial respiration. If breathing is difficult, give oxygen. Get medical aid.
Skin:
Get medical aid. Flush skin with plenty of soap and water for at least 15 minutes while removing contaminated clothing and shoes. Wash clothing before reuse.
Eyes:
Flush eyes with plenty of water for at least 15 minutes, occasionally lifting the upper and lower eyelids. Get medical aid immediately.
2. Handling and Storage
Storage:
Store in a tightly closed container. Store in a cool, dry, well-ventilated area away from incompatible substances.
Handling:
Wash thoroughly after handling. Remove contaminated clothing and wash before reuse. Use with adequate ventilation. Minimize dust generation and accumulation. Avoid contact with eyes, skin, and clothing. Keep container tightly closed. Avoid ingestion and inhalation.

Product Name

2-(2-Hydroxyphenyl)benzothiazole

Synthetic route

2-(2-Hydroxyphenyl)benzothiazole Chemical Properties

2-(2-Hydroxyphenyl)benzothiazole Safety Profile

2-(2-Hydroxyphenyl)benzothiazole Specification

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