4292-92-6 Usage
Description
N-PENTYLCYCLOHEXANE, with the molecular formula C11H22, is a saturated hydrocarbon that features a cyclohexane ring to which a pentyl group is attached. This colorless, odorless liquid is relatively stable and exhibits low toxicity, making it suitable for a range of applications.
Uses
Used in Chemical Production:
N-PENTYLCYCLOHEXANE is utilized as a component in the production of various chemicals, contributing to the synthesis of a wide array of compounds for different industries.
Used in Paints and Coatings Industry:
N-PENTYLCYCLOHEXANE serves as a solvent in the manufacture of paints and coatings, enhancing their properties and aiding in the application process due to its ability to dissolve a variety of substances.
Used in Adhesives Industry:
In the adhesives industry, N-PENTYLCYCLOHEXANE is employed as a solvent to improve the performance of adhesives, facilitating better bonding and adherence to surfaces.
Used in Natural Products Extraction:
N-PENTYLCYCLOHEXANE is also used as a solvent in the extraction of natural products, where its solvent properties help in the efficient isolation of desired components from raw materials.
Check Digit Verification of cas no
The CAS Registry Mumber 4292-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,2,9 and 2 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4292-92:
(6*4)+(5*2)+(4*9)+(3*2)+(2*9)+(1*2)=96
96 % 10 = 6
So 4292-92-6 is a valid CAS Registry Number.
InChI:InChI=1/C11H22/c1-2-3-5-8-11-9-6-4-7-10-11/h11H,2-10H2,1H3
4292-92-6Relevant articles and documents
-
Acree,Laforge
, p. 48,50 (1940)
-
Cross-coupling reaction of alkyl halides with alkyl grignard reagents catalyzed by cp-iron complexes in the presence of 1,3-butadiene
Iwasaki, Takanori,Shimizu, Ryohei,Imanishi, Reiko,Kuniyasu, Hitoshi,Kambe, Nobuaki
supporting information, p. 763 - 766 (2018/05/29)
Iron-catalyzed cross-coupling reaction of alkyl halides with alkyl Grignard reagents by the combined use of cyclopentadienyl ligand and 1,3-butadiene additive is described. The reaction smoothly proceeds at room temperature using unactivated alkyl bromides and fluorides via non-radical mechanism, which is in sharp contrast with hitherto known Fe-catalyzed cross-coupling reactions of alkyl halides.
Catalytic hydrogenation of aromatic rings catalyzed by Pd/NiO
Wang, Yanan,Cui, Xinjiang,Deng, Youquan,Shi, Feng
, p. 2729 - 2732 (2014/01/06)
A simple and efficient heterogeneous palladium catalyst was prepared for aromatic ring hydrogenation. The catalyst was prepared by a reduction-deposition method and exhibited high activity and selectivity for the hydrogenation of a variety of substituted aromatic compounds to the corresponding cyclohexane and cyclohexanol derivatives with up to 99% yields. The catalyst was characterized by BET, TEM, XRD, XPS and ICP. Meanwhile the reusability of the catalyst was investigated, and it can be reused for several runs without significant deactivation.
