5-Chlorobenzooxazole-2-thiol

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5-Chlorobenzooxazole-2-thiol Basic information
Product Name:5-Chlorobenzooxazole-2-thiol
Synonyms:5-chloro-2-mercapto-benzoxazol;5-CHLORO-1,3-BENZOXAZOLE-2-THIOL;5-Chloro-2-mercaptobenzoxazine;5-Chlorobenzooxazole-2-thiol;5-Chloro-2,3-dihydrobenzoxazole-2-thione;5-Chlorobenzoxazole-2(3H)-thione;2(3H)-Benzoxazolethione, 5-chloro-;2-Benzoxazolethiol, 5-chloro-
CAS:22876-19-3
MF:C7H4ClNOS
MW:185.63
EINECS:
Product Categories:Isoxazoles, Oxadiazoles, Oxazoles;OxazolesHeterocyclic Building Blocks;Building Blocks;Halogenated Heterocycles;Heterocyclic Building Blocks;Oxazoles
Mol File:22876-19-3.mol
5-Chlorobenzooxazole-2-thiol Structure
5-Chlorobenzooxazole-2-thiol Chemical Properties
Melting point 280-285 °C(lit.)
Boiling point 278.7±42.0 °C(Predicted)
density 1.57±0.1 g/cm3(Predicted)
storage temp. 2-8°C
pka10.45±0.20(Predicted)
AppearanceLight yellow to brown Solid
InChI1S/C7H4ClNOS/c8-4-1-2-6-5(3-4)9-7(11)10-6/h1-3H,(H,9,11)
InChIKeyBOBIZYYFYLLRAH-UHFFFAOYSA-N
SMILESSc1nc2cc(Cl)ccc2o1
CAS DataBase Reference22876-19-3(CAS DataBase Reference)
Safety Information
Hazard Codes Xn
Risk Statements 22-36/37/38
Safety Statements 26-36
WGK Germany 3
RTECS DM4760000
HazardClass IRRITANT
HS Code 2934999090
Storage Class11 - Combustible Solids
Hazard ClassificationsAcute Tox. 4 Oral
Eye Irrit. 2
Skin Irrit. 2
STOT SE 3
Toxicitymouse,LD50,intraperitoneal,120mg/kg (120mg/kg),Medicinal Chemistry: A Series of Monographs. Vol. 4(1), Pg. 337, 1964.
MSDS Information
ProviderLanguage
SigmaAldrich English
5-Chlorobenzooxazole-2-thiol Usage And Synthesis
Uses5-Chloro-2-mercaptobenzoxazole may be used in the synthesis of 5-chloro-2-(4-methyl-1-piperazinyl)benzoxazole and 5-chloro-2-morpholin-4-yl-1,3-benzoxazole.
General Description5-Chloro-2-mercaptobenzoxazole can be synthesized by reacting amino-4-chlorophenol, potassium hydroxide and carbon disulfide in ethanol.
Synthesis
Potassium ethylxanthate

140-89-6

2-Amino-4-chlorophenol

95-85-2

5-Chlorobenzooxazole-2-thiol

22876-19-3

Synthesis of compound 19: A mixture of potassium ethylxanthate (13.4 g, 84.0 mmol) and 4-chloro-2-aminophenol (10 g, 69.6 mmol) was dissolved in anhydrous ethanol (200 mL). The reaction mixture was stirred under reflux conditions overnight. After completion of the reaction, it was cooled to room temperature and the solvent was removed by evaporation under reduced pressure. The residue was dissolved in water (200 mL) and the pH was adjusted with acetic acid (HOAc) to 5. A solid product was precipitated, filtered and dried to afford 5-chloro-2-mercaptobenzoxazole (12.8 g, 99.1% yield).

References[1] Patent: US2011/224269, 2011, A1. Location in patent: Page/Page column 21
[2] Patent: CN106478537, 2017, A. Location in patent: Paragraph 0025; 0026; 0037; 0038; 0048; 0049; 0062-0064
[3] Patent: US2016/168138, 2016, A1. Location in patent: Paragraph 0142-0143
[4] Patent: CN106632121, 2017, A. Location in patent: Paragraph 0031; 0032
[5] Bioorganic and Medicinal Chemistry Letters, 2013, vol. 23, # 3, p. 907 - 911
Tag:5-Chlorobenzooxazole-2-thiol(22876-19-3) Related Product Information
Benzoxazole Famoxadone Sulfamethoxazole Fenoxaprop-p-ethyl ISOXAFLUTOLE Isoxazole 2-Mercaptobenzoxazole Difluorochloromethane 5-Chlorobenzoxazole 6-Chloro-2-benzoxazolethiol 5-Chlorobenzooxazole-2-thiol Ethyl 2-[(5-chloro-1,3-benzoxazol-2-yl)sulfanyl]acetate S-(5-Chloro-1,3-benzoxazol-2-yl) 4-chlorobenzenecarbothioate 5-Chloro-1,3-benzoxazol-2-yl 5-nitro-2-pyridinyl sulfide S-(5-Chloro-1,3-benzoxazol-2-yl) 2-chlorobenzenecarbothioate 5-Chloro-1,3-benzoxazol-2-yl 4-chlorobenzyl sulfide 5-Chloro-1,3-benzoxazol-2-yl 3-chlorobenzyl sulfide 5-Chloro-7-methylbenzo[d]oxazole-2-thiol