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2-Bromo-10H-phenothiazine

CAS No.
66820-95-9
Chemical Name:
2-Bromo-10H-phenothiazine
Synonyms
2-Bromo-10H-phenothiazine;2-Bromo-10H-phgenothiazine;10H-Phenothiazine, 2-bromo-
CBNumber:
CB33367585
Molecular Formula:
C12H8BrNS
Molecular Weight:
278.17
MDL Number:
MOL File:
66820-95-9.mol
MSDS File:
SDS
Last updated:2026-05-28 04:57:36

2-Bromo-10H-phenothiazine Properties

storage temp. Sealed in dry,Room Temperature
Appearance Light yellow to yellow Solid

SAFETY

Risk and Safety Statements

Symbol(GHS)  Exclamation Mark (GHS07)
GHS07
Signal word  Warning
Hazard statements  H302
Precautionary statements  P280-P305+P351+P338
REACH Registrations Active

2-Bromo-10H-phenothiazine price

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
Matrix Scientific 301934 2-Bromo-10H-phenothiazine 66820-95-9 250.00mg $97 2026-05-19 Buy
Matrix Scientific 301934 2-Bromo-10H-phenothiazine 66820-95-9 1.00g $350 2026-05-19 Buy
Matrix Scientific 301934 2-Bromo-10H-phenothiazine 66820-95-9 5.00g $796 2026-05-19 Buy
Synthonix B56437 2-Bromo-10H-phenothiazine 97% 66820-95-9 50mg $53 2026-05-06 Buy
Synthonix B56437 2-Bromo-10H-phenothiazine 97% 66820-95-9 100mg $60 2026-05-06 Buy
Product number Packaging Price Buy
301934 250.00mg $97 Buy
301934 1.00g $350 Buy
301934 5.00g $796 Buy
B56437 50mg $53 Buy
B56437 100mg $60 Buy

2-Bromo-10H-phenothiazine Chemical Properties, Uses, Production

Uses

2-Bromo-10H-phenothiazine is a useful reactant in organic synthesis.

Synthesis

4-BROMO-2-CHLORO-1-IODOBENZENE

31928-47-9

Ethanethioic acid,S-[2-(acetylamino)phenyl] ester

1204-55-3

2-Bromo-10H-phenothiazine

66820-95-9

General procedure for the synthesis of 2-bromo-10H-phenothiazine from 4-bromo-2-chloroiodobenzene and S-(2-acetamidophenyl) thioacetate: to a 25 mL oven-dried, ground-mouth test tube fitted with a stirrer, was added sequentially S-(2-acetamidophenyl) thioacetate (0.5 mmol), 4-bromo-2-chloroiodobenzene (0.6 mmol), Cs2CO3 (2.0 mmol) and DMF (3 mL). The test tube was sealed with a sleeve rubber stopper, evacuated and replaced with argon, and this operation was repeated three times. The reaction mixture was stirred at 130°C for 10 hours. After completion of the reaction, it was cooled to room temperature, the reaction was quenched with water (20 mL) and extracted three times with ethyl acetate (20 mL). The organic layers were combined, dried with anhydrous MgSO4 and subsequently concentrated under reduced pressure on a rotary evaporator. Finally, the residue was purified by silica gel column chromatography using gradient elution (eluent: petroleum ether/ethyl acetate) to afford the target product 2-bromo-10H-phenothiazine.

References

[1] Synthetic Communications, 2017, vol. 47, # 7, p. 710 - 715

2-Bromo-10H-phenothiazine Preparation Products And Raw materials

2-Bromo-10H-phenothiazine Suppliers

Global Suppliers ( 26)
Supplier Tel Email Country ProdList Advantage
Cool Pharm, Ltd 021-60455363 18019463053 sales@coolpharm.com China 8455 58
ShangHai Movin Pharmaceutical Co., Ltd. 13681854265 info@moenpharm.com China 488 55
Aikon International Limited 025-58859352 19370895928 sales01@aikonchem.com China 15078 58
Shanghai Benso Pharmaceutical Technology Co., Ltd. 13023173052 248775804@qq.com China 4917 58
Shanghai Jizhi Biochemical Technology Co. Ltd. 021-4009004166/18616739031 18616739031 3007523370@qq.com China 40000 58
Henan Alpha Chemical Co., Ltd. 0371-55055611 18137792234 3957071458@qq.com China 9969 58
sgtlifesciences pvt ltd +91-8790379245 dj@sgtlifesciences.com China 12351 58
Shanxi Xuanran Import and Export Trade Co., Ltd. +8617735180244 mike_yan@xuanranglobal.com CHINA 4011 58
Energy Chemical 021-58432009 400-005-6266 marketing@energy-chemical.com China 44871 58
Shanghai Haohong Pharmaceutical Co., Ltd. 400-8210725 4008210725 malulu@leyan.com China 39796 58

2-Bromo-10H-phenothiazine Spectrum

2-Bromo-10H-phenothiazine 2-Bromo-10H-phgenothiazine 10H-Phenothiazine, 2-bromo- 66820-95-9