26420-79-1

Basic information

• Product Name: 1-(BENZYLOXY)-3-CHLOROPROPANE
• Synonyms: 1-(BENZYLOXY)-3-CHLOROPROPANE;1-Chloro-3-benzyloxypropane;Benzyl 3-chloropropyl ether;Benzyl(3-chloropropyl) ether;Nsc6169;3-Chloro-1-benzyloxypropane
• CAS NO: 26420-79-1
• Molecular Formula: C₁₀H₁₃ClO
• Molecular Weight: 184.66
• Mol File: 26420-79-1.mol
• Article Data: 16

Chemical Properties

• Boiling Point: 250 °C at 760 mmHg
• Flash Point: 109.9 °C
• Appearance: /
• Density: 1.067 g/cm³
• Vapor Pressure: 0.0351mmHg at 25°C
• Refractive Index: 1.509
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-(BENZYLOXY)-3-CHLOROPROPANE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(BENZYLOXY)-3-CHLOROPROPANE(26420-79-1)
• EPA Substance Registry System: 1-(BENZYLOXY)-3-CHLOROPROPANE(26420-79-1)

Safety Data

• Hazardous Substances Data: 26420-79-1(Hazardous Substances Data)

Usage

General Description

1-(Benzyloxy)-3-chloropropane, also known as benzyloxychloropropane, is a chemical compound consisting of a benzene ring attached to a propyl chain with a chlorine atom. It is commonly used in organic synthesis as a reagent for the introduction of the benzyloxy group into various organic compounds. 1-(BENZYLOXY)-3-CHLOROPROPANE is also used in the production of pharmaceuticals, agrochemicals, and other fine chemicals. It is important to handle this chemical with caution and follow safety protocols as it may be hazardous if not handled properly.

InChI:InChI=1/C10H13ClO/c11-7-4-8-12-9-10-5-2-1-3-6-10/h1-3,5-6H,4,7-9H2

Upstream product

• 4799-68-2 3-benzyloxypropan-1-ol 
• 100-39-0 benzyl bromide 
• 627-30-5 1-chloro-3-hydroxypropane 
• 100-44-7 benzyl chloride 
• 504-63-2 trimethyleneglycol 
• 55791-06-5 benzyl mesylate 
• 54314-84-0 1-[(3-bromopropoxy)methyl]-benzene 
• 1189748-23-9 C₈H₉ClO₂ 
• 32315-10-9 bis(trichloromethyl) carbonate 
• 121-44-8 triethylamine 
• 100-51-6 benzyl alcohol 

Downstream Products

• 82258-55-7 Ethyl 5-benzyloxy-2-(ethoxycarbonyl)pentanoate 
• 85174-51-2 4-(benzyloxy)butyronitrile 
• 184094-92-6 bis-(3-benzyloxy-propyl)-sulfide 
• 5375-00-8 3-benzyloxypropyl iodide 
• 74287-04-0 2-(4-Benzyloxy-1-phenyl-butyl)-pyridine 
• 143703-95-1 3-(benzyloxy)propyl 4-nitrophenyl ether 
• 85690-23-9 4-(3-benzyloxypropyl)-4,9-dihydrothieno<2,3-c>-2-benzothiepin-4-ol 
• 82212-55-3 2-fluoromethyl-2-amino-5-benzyloxy-pentanenitrile 
• 116527-73-2 1,1-diethoxy-3,3-(diethoxycarbonyl)-6-benzyloxyhexan 
• 126036-01-9 6-benzyloxy-2-methylhexene 
• 61103-84-2 benzyl hexyl ether 
• 90812-83-2 4-benzyloxy-1-(furan-3'-yl)butan-1-one 
• 160560-18-9 1-(furan-3'-yl)-2-phenylethan-1-one 
• 90812-84-3 4-benzyloxy-1-<2'-(furan-3''-oyl)furan-3'-yl>butan-1-one 

Relevant articles and documents

Selective alkyl ether cleavage by cationic bis(phosphine)iridium complexes

Catalysts capable of heterolytic silane activation have been successfully applied to the conversion of alkyl ethers to silyl ethers via C-O bond cleavage. The previously-reported cationic pincer-supported iridium complex for this transformation suffers fr

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Activation of primary aliphatic alcohols with triphosgene and triethylamine mixtures afforded either alkyl chloride or diethylcarbamate products, and the switch in selectivity appeared to be driven by sterics. The reaction conditions to achieve this highly useful transformation were unexceptionally mild and readily tolerated by a wide range of sensitive functionalities.