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1126-75-6

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1126-75-6 Usage

Description

(2-methylpropoxy)benzene, also known as isobutylbenzene, is a colorless liquid chemical compound with the molecular formula C10H14. It possesses a sweet, floral odor and is commonly utilized in various industrial applications.

Uses

Used in Industrial Cleaners:
(2-methylpropoxy)benzene is used as a solvent in the production of industrial cleaners due to its ability to dissolve a wide range of substances, making it effective in removing dirt and stains.
Used in Perfumes and Personal Care Products:
(2-methylpropoxy)benzene is used as a fragrance ingredient in perfumes and personal care products, providing a sweet, floral scent that enhances the overall aroma of these products.

Check Digit Verification of cas no

The CAS Registry Mumber 1126-75-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,2 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1126-75:
(6*1)+(5*1)+(4*2)+(3*6)+(2*7)+(1*5)=56
56 % 10 = 6
So 1126-75-6 is a valid CAS Registry Number.

1126-75-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methylpropoxybenzene

1.2 Other means of identification

Product number -
Other names Isobutyl-phenyl-aether

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1126-75-6 SDS

1126-75-6Relevant articles and documents

Radiosynthesis of 1-iodo-2-[11C]methylpropane and 2-methyl-1-[11C]propanol and its application for alkylation reactions and C―C bond formation

Rotteveel, Lonneke,Poot, Alex J.,Funke, Uta,Peko?ak, Aleksandra,Filp, Ulrike,Lammertsma, Adriaan A.,Windhorst, Albert D.

, p. 566 - 576 (2017)

The multitude of biologically active compounds requires the availability of a broad spectrum of radiolabeled synthons for the development of positron emission tomography (PET) tracers. The aim of this study was to synthesize 1-iodo-2-[11C]methylpropane and 2-methyl-1-[11C]propanol and investigate the use of these reagents in further radiosynthesis reactions. 2-Methyl-1-[11C]propanol was obtained with an average radiochemical yield of 46?±?6% d.c. and used with fluorobenzene as starting material. High conversion rates of 85?±?4% d.c. could be observed with HPLC, but large precursor amounts (32?mg, 333?μmol) were needed. 1-Iodo-2-[11C]methylpropane was synthesized with a radiochemical yield of 25?±?7% d.c. and with a radiochemical purity of 78?±?7% d.c. The labelling agent 1-iodo-2-[11C]methylpropane was coupled to thiophenol, phenol and phenylmagnesium bromide. Average radiochemical conversions of 83% d.c. for thiophenol, 40% d.c. for phenol, and 60% d.c. for phenylmagnesium bromide were obtained. In addition, [11C]2-methyl-1-propyl phenyl sulphide was isolated with a radiochemical yield of 5?±?1% d.c. and a molar activity of 346?±?113?GBq/μmol at the end of synthesis. Altogether, the syntheses of 1-iodo-2-[11C]methylpropane and 2-methyl-1-[11C]propanol were achieved and applied as proof of their applicability.

Domino Methylenation/Hydrogenation of Aldehydes and Ketones by Combining Matsubara's Reagent and Wilkinson's Catalyst

Maazaoui, Radhouan,Pin-Nó, María,Gervais, Kevin,Abderrahim, Raoudha,Ferreira, Franck,Perez-Luna, Alejandro,Chemla, Fabrice,Jackowski, Olivier

supporting information, p. 5732 - 5737 (2016/12/14)

The methylenation/hydrogenation cascade reaction of aldehydes or ketones through a domino process involving two ensuing steps in a single pot is realized. The compatibility of Matsubara's reagent and Wilkinson's complex give a combination that allows, under dihydrogen, the transformation of a carbonyl function into a methyl group. This new method is suitable to introduce an ethyl motif from aromatic and aliphatic aldehydes with total chemoselectivity and total retention of α-stereochemical purity. The developed procedure is also extended to the introduction of methyl groups from ketones.

Heterogeneous palladium-catalyzed synthesis of aromatic ethers by solvent-free dehydrogenative aromatization: Mechanism, scope, and limitations under aerobic and non-aerobic conditions

Sutter, Marc,Lafon, Romain,Raoul, Yann,Metay, Estelle,Lemaire, Marc

supporting information, p. 5902 - 5916 (2013/09/23)

Starting from cyclohexanone derivatives and alcohols, both non-aromatic precursors, aryl ethers could be synthesized in good yields and with good selectivities in the presence of a catalytic amount of Pd/C, in one step, without added solvent, in a reaction vessel open to air. For less reactive substrates, the addition of 1-octene in a closed system under non-aerobic conditions improved the conversion. In addition, the catalyst could be recycled several times with no decrease in the yield of the aryl ether. The process was also used with tetralone derivatives and polyols. Several reactions were performed to propose a mechanism for this transformation. The formation of an enol ether followed by a dehydrogenation reaction seem to be the key steps of this reaction. Aryl ethers were prepared in good yields and with good selectivities in a solvent-free and heterogeneous catalytic dehydrogenative alkylation of cyclohexanones with various alcohols. Three different complementary routes were used, and for the first time, non-aerobic, safe conditions could be used. Moreover, the catalyst could be recycled several times with no decrease in the yield of the aryl ether. Copyright

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