634193-72-9

Basic information

• Product Name: Bisphenol F 2,3-Dihydroxypropyl (2-Chloro-1-propanol) Ether
• Synonyms: Bisphenol F 2,3-Dihydroxypropyl (2-Chloro-1-propanol) Ether
• CAS NO: 634193-72-9
• Molecular Formula: C19H23ClO5
• Molecular Weight: 366.83592
• Product Categories: Aromatics, Pharmaceuticals, Intermediates & Fine Chemicals
• Mol File: 634193-72-9.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: Bisphenol F 2,3-Dihydroxypropyl (2-Chloro-1-propanol) Ether(CAS DataBase Reference)
• NIST Chemistry Reference: Bisphenol F 2,3-Dihydroxypropyl (2-Chloro-1-propanol) Ether(634193-72-9)
• EPA Substance Registry System: Bisphenol F 2,3-Dihydroxypropyl (2-Chloro-1-propanol) Ether(634193-72-9)

Safety Data

• Hazardous Substances Data: 634193-72-9(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
Bisphenol F 2,3-Dihydroxypropyl (2-Chloro-1-propanol) Ether is used as a therapeutic agent for the treatment of various medical conditions, including prostate cancer. Its chemical properties make it a promising candidate for pharmaceutical applications, where it can potentially help in the development of new drugs and therapies.
Used in Food Packaging Industry:
Bisphenol F 2,3-Dihydroxypropyl (2-Chloro-1-propanol) Ether is also found in resins used as a coating for food contact packaging materials. Its presence in these materials is due to its ability to provide a protective barrier and enhance the durability and safety of the packaging. This application ensures that the packaged food products remain uncontaminated and maintain their quality during storage and transportation.

Upstream product

• 620-92-8 bis-(4-hydroxyphenyl)methane 

Relevant articles and documents

Preparation method of bisphenol F 2222,dihydroxypropyl (2 -chloro -1 - propyl) diethyl ether

The invention discloses a bisphenol F 2222,dihydroxypropyl (2 -chloro -1 - propyl) diethyl ether method which comprises the following steps S1) adding bisphenol F, epichlorohydrin, potassium hydroxide and tetrabutylammonium bromide into a reaction container. S2) The obtained material is diluted with ethyl acetate, then washed with water, the organic phase is separated, and the bisphenol F glycidyl ether is obtained by purification and separation. S3) A mixture of bisphenol F glycidyl ether, tin dichloride dihydrate and diethyl ether is added to the reactor. S4) The obtained material is diluted with ethyl acetate, then washed with water, the organic phase is separated, and the bisphenol F glycidyl ether is obtained by purification and separation. S5) The obtained material and distilled water are added to the reaction vessel to react. S6) The obtained material is extracted and separated by ethyl acetate to obtain an organic phase, and the organic phase is purified and separated to obtain the organic phase. The raw materials are easy to obtain, and the reaction conditions are mild. Target product purity is high, aftertreatment is simple and convenient and green.