Company Details
  • Taizhou Volsen Chemical Co., Ltd.

  •  [Zhejiang,China]
  • Business Type:Manufacturer
  • Main Mark: Americas , Asia , East Europe , Europe , North Europe , Other Markets , West Europe , Worldwide
  • Exporter:91% - 100%
  • Certs:GS, CE, ISO9001, ISO14000
  • Description:Benzoxazole,Synthesis Benzoxazole,Compound of Benzoxazole
Taizhou Volsen Chemical Co., Ltd. Benzoxazole,Synthesis Benzoxazole,Compound of Benzoxazole
Home > Products > Contract Manufacturing > Synthesis of the Benzoxazole Compound

Synthesis of the Benzoxazole Compound

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    Payment Type: L/C,T/T
    Incoterm: FOB,CIF
    Min. Order: 1 Kilogram
    Delivery Time: 25 Days

Basic Info

Model No.: Benzoxazole

Grade Standard: Medicine Grade

State: Solid

Additional Info

Packaging: 25KGS/DRUM

Productivity: Custom Manufacturing


Transportation: Air

Place of Origin: CHINA

Supply Ability: In stock

Product Description

Benzoxazole is a Compound in pale yellow solid, which has the Molecular Formula: C11H7CIOMolecular Weight: 190.6.Benzoxazole purity > 98%, is not in stock, would be available through custom synthesis. Minimum 100 gram order is requested. Current shipping out time is about 30 days after order is received.

Thera Category:

Cas No.:



Molecular Formula: C11H7CIO

Molecular Weight: 190.63

Purity: NLT98%

Appearance: Pale yellow solid

Specifications: Available on request

Packing:Export worthy packing

Material Safety Data Sheet:Available on request

Procedure: To an oven-dried, argon-cooled flask (100 mL capacity) equipped with magnetic stir

bar was added 1 (2.01 g, 10 mmole, 1.0 equiv) and dioxane (20 mL). To this solution was slowly
added acid chloride 2 (1.91 g, 10 mmole, 1.0 equiv). The solution was diluted with dioxane (5
mL), methanesulfonic acid (3, 2.98g, 30 mmole, 3.1 equiv) were added. The reaction was slowly
heated to reflux (100 °C) and maintained at reflux for 2.5 hours. The analysis of the reaction
mixture using thin layer chromatography revealed complete consumption of the starting
materials 1 and 2. The reaction was cooled to room temperature and dioxane was removed
using rotary evaporator. The reaction mixture was diluted with ethyl acetate (ca. 50 mL) and
was slowly poured into sat. NaHCO3 solution. The organic layer was washed with distilled water
(2 X 50 mL) and was dried using anhydrous Na2SO4. Evaporation of ethyl acetate under
reduced pressure lead to the isolation of the desired product in crude form. Purification using
silica gel flash column chromatography lead to the isolation of the pure chemical (2.51 g, 74%
yield) as a pale yellow solid.

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  • Synthesis of the Benzoxazole Compound
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