5078-75-1 Usage
Description
(3-Methylcyclopentyl)benzene, also known as 3-Methyl-1-cyclopentylbenzene, is a chemical compound with the molecular formula C12H16. It consists of a benzene ring with a cyclopentyl group attached at the 3-position. (3-Methylcyclopentyl)benzene is a colorless liquid at room temperature and is used in the production of chemicals and pharmaceuticals.
Uses
Used in Chemical Production:
(3-Methylcyclopentyl)benzene is used as an intermediate in the synthesis of various chemicals, contributing to the development of new compounds with potential applications in different industries.
Used in Pharmaceutical Industry:
(3-Methylcyclopentyl)benzene is used as a building block in the production of pharmaceuticals, aiding in the creation of new drugs and medications.
Used as a Solvent:
(3-Methylcyclopentyl)benzene is used as a solvent in various industrial processes, facilitating chemical reactions and improving the efficiency of manufacturing operations.
Used in Research and Development:
(3-Methylcyclopentyl)benzene is utilized in research and development settings to study its properties and explore its potential applications in new areas.
Note: It is important to handle (3-Methylcyclopentyl)benzene with care, as it is considered a hazardous substance and can cause skin and eye irritation.
Check Digit Verification of cas no
The CAS Registry Mumber 5078-75-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,0,7 and 8 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 5078-75:
(6*5)+(5*0)+(4*7)+(3*8)+(2*7)+(1*5)=101
101 % 10 = 1
So 5078-75-1 is a valid CAS Registry Number.
5078-75-1Relevant articles and documents
A tin hydride designed to facilitate removal of tin species from products of stannane-mediated radical reactions
Clive, Derrick L. J.,Wang, Jian
, p. 1192 - 1198 (2007/10/03)
The stannane 1, which is simple to prepare, behaves like the conventional reagents Bu3SnH and Ph3SnH in standard free radical reactions, but with the special characteristic that the tin-containing byproducts are easily and very largely removed by mild hydrolysis (LiOH-water-THF or TsOH-water-THF), which converts them into base-soluble (aqueous NaHCO3) materials. The performance of stannane 1 was evaluated for a range of radical reactions involving halides, selenides, Barton-McCombie deoxygenation, and enyne cyclization. In several cases the effectiveness of the workup procedure in removing tin species was monitored by 1H NMR.
Organoyttrium-catalyzed cyclization of substituted 1,5- and 1,6-dienes
Molander, Gary A.,Hoberg, John O.
, p. 3123 - 3125 (2007/10/02)
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