929-05-5

Usage

Uses

Used in Flavor and Fragrance Industry:
1-Butenyl Ethyl Ether is used as a flavor and fragrance ingredient for its distinctive sweet, fruity scent, enhancing the sensory experience in various consumer products such as perfumes, soaps, and cosmetics.
Used in Industrial Applications:
1-Butenyl Ethyl Ether serves as a solvent in a range of industrial processes, leveraging its chemical properties to facilitate specific reactions or processes within the industry.
Safety Considerations:
Given its potential to cause harm if ingested, inhaled, or upon skin contact, 1-Butenyl Ethyl Ether necessitates the implementation of proper safety measures during its handling and storage to mitigate risks of irritation to the respiratory system and skin.

InChI:InChI=1/C6H12O/c1-3-5-6-7-4-2/h5-6H,3-4H2,1-2H3/b6-5+

Upstream product

• 3658-95-5 1,1-diethoxybutane 
• 542-16-5 dianilunium sulphate 
• 121-57-3 4-aminobenzene sulfonic acid 
• 123-72-8 butyraldehyde 
• 122-51-0 orthoformic acid triethyl ester 

Downstream Products

• 99861-37-7 2-(α-ethoxy-furfuryl)-butyraldehyde 
• 5870-82-6 1,1,3-triethoxy-butane 
• 869-33-0 1,1,3,5-tetraethoxy-hexane 
• 870-82-6 1,1,3,5,7-pentaethoxy-octane 
• 100392-96-9 3-ethoxy-2-ethyl-butyraldehyde diethylacetal 
• 103649-14-5 3-ethoxy-2-ethyl-hex-4t-enal 
• 105540-72-5 3-ethoxy-2-ethyl-octa-4t,6t-dienal 
• 2983-24-6 1,2-dibromo-1-ethoxybutane 
• 99850-88-1 3-ethoxy-2-ethyl-hexanal 
• 30989-69-6 2-(diethoxymethyl)-1,1-diethoxybutane 
• 56585-20-7 (4-Diethoxymethyl-3-isopropoxy-hexyl)-benzene 
• 56585-21-8 2-Ethyl-5-pentyl-2-pentenal 
• 13610-87-2 2-(4-chloro-benzenesulfonyl)-3-ethoxy-4-ethyl-[1,2]thiazetidine 1-oxide 
• 52114-60-0 3-Ethoxy-4-ethyl-cyclobutane-1,1,2,2-tetracarbonitrile 

Relevant academic research and scientific papers

A short high yielding synthesis of the potent anti-VZV carbocyclic nucleoside analogue carba-BVDU

A short high yielding synthesis of the potent anti-varicella-zoster virus (VZV) carbocyclic nucleoside analogue carba-BVDU 1 starting from aminodiol 2 is described. Reaction of 2 with acyl carbamate 3 and subsequent ring closure under acidic conditions afforded 5-ethyl-2'-deoxy-4'a-carbauridine 5. In situ acetylation of 5 afforded 3',5'-di-O-acetyl-5-ethyl-2'-deoxy-4'a-carbauridine 6 in 78% overall yield from 2. Radical bromination of 6 with either bromine or NBS and subsequent treatment with triethylamine gave an efficient conversion to 3',5'-di-O-acetyl-5-(E)-(2-bromovinyl)-2'-deoxy-4'a- carbauridine 7. Deacetylation of 7 afforded 1 in an overall 45-53% yield from 2.

Synthesis and cyanation of octaalkylporphyrins using electrochemical methods

The total synthesis of octaalkylporphyrins (ethyl, buthyl, isopropyl) and the cyanation of the meso (methine bridge) positions have been achieved using electrochemical methods.The coupled products (diketals) from anodic oxidation of aldehydes enol ethers (or enamines) in methanol, on subsequent reaction with benzyl carbamate undergo cyclisation to N-carbobenzyloxypyrroles.Deprotection and reaction with formaldehyde afforded the corresponding porphyrins.Electrolysis of zinc-octaethylporphyrin in dimethylformamide in the presence of cyanide at various concentrations and potentials (+0.45 to 0.9 V/SCE) gave mono- to tetracyano-octaethylporphyrins which were fully caracterized.