3311-94-2

Basic information

• Product Name: 1,1'-(4-chloro-1-butenylidene)bis[4-fluorobenzene]
• Synonyms: 1,1'-(4-chloro-1-butenylidene)bis[4-fluorobenzene];Einecs 221-996-5;4,4-(4-chlorobut-1-ene-1,1-diyl)bis(fluorobenzene)
• CAS NO: 3311-94-2
• Molecular Formula: C₁₆H₁₃ClF₂
• Molecular Weight: 278.7242264
• EINECS: 221-996-5
• Mol File: 3311-94-2.mol
• Article Data: 3

Chemical Properties

• Boiling Point: 375.5°Cat760mmHg
• Flash Point: 209.9°C
• Appearance: /
• Density: 1.195g/cm³
• CAS DataBase Reference: 1,1'-(4-chloro-1-butenylidene)bis[4-fluorobenzene](CAS DataBase Reference)
• NIST Chemistry Reference: 1,1'-(4-chloro-1-butenylidene)bis[4-fluorobenzene](3311-94-2)
• EPA Substance Registry System: 1,1'-(4-chloro-1-butenylidene)bis[4-fluorobenzene](3311-94-2)

Safety Data

• Hazardous Substances Data: 3311-94-2(Hazardous Substances Data)

Usage

Explanation

The compound is composed of 20 carbon atoms, 14 hydrogen atoms, 1 chlorine atom, and 2 fluorine atoms.

Explanation

The compound consists of two 4-fluorobenzene rings connected by a 4-chloro-1-butenylidene group.

Explanation

It contains carbon and hydrogen atoms, classifying it as an organic compound.

Explanation

The compound has four fluorine atoms within its structure.

Explanation

The compound has a butenylidene group (-CH=CH-CH=) connecting the two 4-fluorobenzene rings.

Explanation

The compound is used in the production of various industrial products, including polymers, resins, and dyes.

Explanation

Due to its unique chemical structure, the compound has potential uses in the pharmaceutical and agricultural industries.

Explanation

Researchers and chemists are interested in the compound because of its unique chemical structure and its potential applications in various fields.

Chemical structure

1,1'-(4-chloro-1-butenylidene)bis[4-fluorobenzene]

Organic compound

Yes

Contains fluorine atoms

4

Contains chlorine atom

1

Contains butenylidene group

Yes

Industrial applications

Polymers, resins, and dyes

Potential applications

Pharmaceutical and agricultural industries

Research interest

Unique chemical structure and potential uses

Upstream product

• 3874-54-2 4-(4-fluorophenyl)-4-oxo-n-butyl chloride 
• 460-00-4 1-Bromo-4-fluorobenzene 
• 51787-80-5 δ-Hydroxy-δ-bis(p-fluorophenyl)butyl chloride 
• 352-13-6 4-flourophenylmagnesium bromide 

Downstream Products

• 77294-02-1 2-[4,4-Bis-(4-fluoro-phenyl)-but-3-enyl]-1,2,3,4,6,7,12,12a-octahydro-pyrazino[1',2':1,6]pyrido[3,4-b]indole 
• 57642-91-8 4-(4-Benzamidopiperid-1-yl)-1,1-(di-p-fluorophenyl)but-1-ene 
• 91830-22-7 1'-[4,4-bis(4-fluorophenyl)-3-butenyl]-5-chlorospiro[benzofuran-2(3H)4'-piperidine]oxalate 

Relevant articles and documents

Ring-opening reaction of methylenecyclopropanes with LiCl, LiBr or NaI in acetic acid

The methylenecyclopropanes 1 react with LiCl, LiBr or NaI at 80°C to give the corresponding gem-disubstituted homoallylic halides 2 in good to excellent yields in acetic acid. In some cases, the ring-opening reaction can be completed within 5 min to give

Neurotropic and psychotropic agents. LXVII. 1 [4,4 bis(4 fluorophenyl)butyl] 4 hydroxy 4 (3 trifluoromethyl 4 chlorophenyl)piperidine and related compounds: new synthetic approaches

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