6334-96-9

Basic information

• Product Name: BIS(4-CHLOROBUTYL) ETHER
• Synonyms: 4-Chlorobutyl Ether 4,4'-Dichlorobutyl Ether 4,4'-Dichlorodibutyl Ether;1,9-Dichloro-5-oxanonane;4-Chlorobutyl ether 98%;1,1’-oxybis(4-chloro-butan;1,1’-oxybis(4-chlorobutane);1,1’-oxybis[4-chloro-butan;1,1’-oxydi-4-chlorobutane;1,1'-Oxydi-4-chlorobutane
• CAS NO: 6334-96-9
• Molecular Formula: C₈H₁₆Cl₂O
• Molecular Weight: 199.12
• EINECS: 228-713-4
• Product Categories: C2 to C8;Chemical Synthesis;Ethers;Organic Building Blocks;Oxygen Compounds;Building Blocks
• Mol File: 6334-96-9.mol
• Article Data: 9

Chemical Properties

• Boiling Point: 129-131 °C10 mm Hg(lit.)
• Flash Point: >230 °F
• Appearance: COLORLESS LIQUID
• Density: 1.081 g/mL at 25 °C(lit.)
• Vapor Pressure: 0.0275mmHg at 25°C
• Refractive Index: n20/D 1.459(lit.)
• Storage Temp.: Refrigerator
• Solubility: Chloroform (Slightly), Ethyl Acetate (Slightly), Methanol (Slightly)
• BRN: 1739861
• CAS DataBase Reference: BIS(4-CHLOROBUTYL) ETHER(CAS DataBase Reference)
• NIST Chemistry Reference: BIS(4-CHLOROBUTYL) ETHER(6334-96-9)
• EPA Substance Registry System: BIS(4-CHLOROBUTYL) ETHER(6334-96-9)

Safety Data

• Hazard Codes: Xn
• Statements: 22-36/37/38
• Safety Statements: 26-36
• RIDADR: UN 3334
• WGK Germany: 3
• RTECS: KN0400000
• TSCA: Yes
• Hazardous Substances Data: 6334-96-9(Hazardous Substances Data)

Usage

Chemical Properties

Clear Colourless Oil

Uses

Different sources of media describe the Uses of 6334-96-9 differently. You can refer to the following data:
1. Bis(4-chlorobutyl) Ether is used in the alkylation of anthracene-cyanoacrylic Diels-Alder adducts.
2. 4-Chlorobutyl ether is generally used as an ether-containing linker while synthesizing organic compounds.

InChI:InChI=1/C8H16Cl2O/c9-5-1-3-7-11-8-4-2-6-10/h1-8H2

Upstream product

• 109-99-9 tetrahydrofuran 
• 75-44-5 phosgene 
• 928-51-8 4-Chloro-1-butanol 
• 110-63-4 Butane-1,4-diol 
• 5435-44-9 (E)-3-Ureido-but-2-enoic acid ethyl ester 
• 10025-87-3 trichlorophosphate 
• 7664-93-9 sulfuric acid 
• 7719-09-7 thionyl chloride 
• 71-36-3 butan-1-ol 
• 107-07-3 2-chloro-ethanol 
• 627-30-5 1-chloro-3-hydroxypropane 
• 78-83-1 2-methyl-propan-1-ol 
• 123-51-3 i-Amyl alcohol 
• 64-17-5 ethanol 

Downstream Products

• 5392-06-3 6-oxa-undecanedinitrile 
• 946-02-1 4-chlorobutyl benzoate 
• 110-56-5 1,4-dichlorobutane 
• 55333-95-4 7,12,17-Trioxa-1,23-tricosandiol Dimesylat 
• 3491-13-2 Bis-(4-<4-amino-phenoxy>-butyl)ether 
• 149697-40-5 C₈Cl₂F₁₆O 
• 183293-82-5 6-(5-carboxy-5-methyl-hexyloxy)-2,2-dimethyl-hexanoic acid 
• 463-31-0 5-(4-fluoro-butoxy)-valeronitrile 
• 1044741-19-6 6-(4-chlorobutoxy)-2,2-dimethylhexanoic acid 
• 109-99-9 tetrahydrofuran 
• 3403-82-5 bis(4-hydroxybutyl)-ether 
• 77376-42-2 4-benzyloxy-2-(9-hydroxy-5-oxanonyloxy)benzoic acid lactone 
• 593-22-6 (4-chloro-butyl)-(4-fluoro-butyl)-ether 

Relevant articles and documents

Electrospray ionization mass spectrometry: A powerful tool to investigate the oligomerization mechanism of tetrahydrofuran by phosphoryl chloride

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ETHER COMPOUNDS AND COMPOSITIONS FOR CHOLESTEROL MANAGEMENT AND RELATED USES

The present invention relates to novel ether compounds, compositions comprising ether compounds, and methods useful for treating and preventing cardiovascular diseases, dyslipidemias, dysproteinemias, and glucose metabolism disorders comprising administering a composition comprising an ether compound. The compounds, compositions, and methods of the invention are also useful for treating and preventing Alzheimer's Disease, Syndrome X, peroxisome proliferator activated receptor-related disorders, septicemia, thrombotic disorders, obesity, pancreatitis, hypertension, renal disease, cancer, inflammation, and impotence. In certain embodiments, the compounds, compositions, and methods of the invention are useful in combination therapy with other therapeutics, such as hypocholesterolemic and hypoglycemic agents.

Reductive cleavage of epoxides with zinc borohydride supported on AIPO4

To whom correspondence should be addressed Reductive cleavage of styrene oxide and epichlorohydrin to alcohols have been achieved using zinc borohydride supported on AlPO4. In the styrene oxide reductive cleavage, Zn(BH4)2 supported on AlPO4 is a better catalyst than Zn(BH4)2/SiO2 previously described.