7510-27-2 Usage
Uses
Used in Organic Synthesis:
(1Z)-1-butoxybut-1-ene is used as a chemical intermediate for the production of various products such as surfactants, detergents, and lubricants. Its unique structure allows it to be a key component in the synthesis of these compounds.
Used in Chemical Reactions:
(1Z)-1-butoxybut-1-ene is used as a solvent in chemical reactions. Its ability to dissolve a wide range of substances makes it a valuable asset in various chemical processes.
Used in Food and Beverage Industry:
(1Z)-1-butoxybut-1-ene is used as a flavor and fragrance ingredient in the food and beverage industry. Its unique properties allow it to enhance the taste and aroma of various products.
Used in Surfactant Production:
(1Z)-1-butoxybut-1-ene is used as a chemical intermediate in the production of surfactants. Surfactants are compounds that lower the surface tension between two liquids or between a liquid and a solid, making them essential in various industries such as cosmetics, pharmaceuticals, and cleaning products.
Used in Detergent Production:
(1Z)-1-butoxybut-1-ene is used as a chemical intermediate in the production of detergents. Detergents are cleaning agents that remove dirt, grease, and stains from various surfaces, making them a crucial component in household and industrial cleaning products.
Used in Lubricant Production:
(1Z)-1-butoxybut-1-ene is used as a chemical intermediate in the production of lubricants. Lubricants are substances that reduce friction between two surfaces in contact, making them essential in various industries such as automotive, machinery, and manufacturing.
Check Digit Verification of cas no
The CAS Registry Mumber 7510-27-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,1 and 0 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 7510-27:
(6*7)+(5*5)+(4*1)+(3*0)+(2*2)+(1*7)=82
82 % 10 = 2
So 7510-27-2 is a valid CAS Registry Number.
7510-27-2Relevant academic research and scientific papers
Iridium Pincer-Catalyzed Dehydrogenation of Ethers Featuring Ethylene as the Hydrogen Acceptor
Lyons, Thomas W.,Bzier, David,Brookhart, Maurice
, p. 4058 - 4062 (2015/09/01)
We describe efficient methods to dehydrogenate ethers by using iridium pincer complexes (iPr4Anthraphos)-Ir(H)(Cl), 4, iPr4PC(sp3)P-Ir(H)(Cl), 5, and (iPr4PCP)-Ir(H)(Cl), 6. At 120°C, cyclic ethers were dehydrogenated with tert-butylethylene as the hydrogen acceptor with high turnover numbers (over 400 in many cases). Acyclic ethers such as diethyl ether can also be dehydrogenated catalytically with TONs up to 90. The efficient dehydrogenation of cyclic and acyclic ethers using ethylene as a more practical hydrogen acceptor has been demonstrated for the first time. (Figure Presented)
The (η6-Naphthalene)(η4-cycloocta-1,5-diene)ruthenium(0) Complex as Precursor for Homogeneous and Heterogeneous Catalysts in the Isomerization of Allyl Ethers and Allyl Acetals to Vinyl Derivatives
Pertici, Paolo,Malanga, Corrado,Giuntoli, Anna,Vitulli, Giovanni,Martra, Gianmarco
, p. 587 - 594 (2007/10/03)
The complex (η6-naphthalene(η4-COD)ruthenium(0), I, (COD=cycloocta-1,5-diene), in the presence of acetonitrile, easily catalyzes the isomerization of allyl ethers and allyl acetals, having different steric and electronic features, to
IRIDIUM PENTAHYDRIDE COMPLEX CATALYZED FORMATION OF C-C BOND BY C-H BOND ACTIVATION FOLLOWED BY OLEFIN INSERTION
Lin, Yingrui,Ma, Dawei,Lu, Xiyan
, p. 3249 - 3252 (2007/10/02)
The formation of carbon-carbon bond was found to occur by first carbon-hydrogen bond activation followed by olefin insertion under the catalysis of an iridium pentahydride complex.
