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15890-36-5

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15890-36-5 Usage

Description

4-Isopropylcyclohexanol is a cyclohexanol chemical compound featuring a cyclohexane ring with a hydroxyl group (-OH) and an isopropyl group branching off, known for its unique structure and wide-ranging applications.
Used in Fragrance Industry:
4-Isopropylcyclohexanol is used as a key component in the production of fragrances for its distinctive scent and ability to blend well with other fragrance ingredients.
Used in Chemical Intermediates Manufacturing:
4-Isopropylcyclohexanol is used as a chemical intermediate for synthesizing various compounds, leveraging its reactive functional groups and structural features.
Used as a Solvent:
4-Isopropylcyclohexanol is used as a solvent in certain applications due to its capacity to dissolve a broad spectrum of substances, making it versatile for different industries.
Used in Pharmaceutical Industry:
4-Isopropylcyclohexanol may have potential applications in the pharmaceutical sector, serving as a starting material or intermediate in the development of new drug compounds, owing to its unique chemical structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 15890-36-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,8,9 and 0 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15890-36:
(7*1)+(6*5)+(5*8)+(4*9)+(3*0)+(2*3)+(1*6)=125
125 % 10 = 5
So 15890-36-5 is a valid CAS Registry Number.
InChI:InChI=1/C9H18O/c1-7(2)8-3-5-9(10)6-4-8/h7-10H,3-6H2,1-2H3/t8-,9-

15890-36-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name trans-4-isopropyl cyclohexanol

1.2 Other means of identification

Product number -
Other names 1r-Isopropyl-cyclohexanol-(4t)

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:15890-36-5 SDS

15890-36-5Relevant articles and documents

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Vavon,Callier

, p. 679 (1927)

-

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Macbeth,Winzor

, p. 264 (1939)

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Cobalt-Nanoparticles Catalyzed Efficient and Selective Hydrogenation of Aromatic Hydrocarbons

Murugesan, Kathiravan,Senthamarai, Thirusangumurugan,Alshammari, Ahmad S.,Altamimi, Rashid M.,Kreyenschulte, Carsten,Pohl, Marga-Martina,Lund, Henrik,Jagadeesh, Rajenahally V.,Beller, Matthias

, p. 8581 - 8591 (2019/09/12)

The development of inexpensive and practical catalysts for arene hydrogenations is key for future valorizations of this general feedstock. Here, we report the development of cobalt nanoparticles supported on silica as selective and general catalysts for such reactions. The specific nanoparticles were prepared by assembling cobalt-pyromellitic acid-piperazine coordination polymer on commercial silica and subsequent pyrolysis. Applying the optimal nanocatalyst, industrial bulk, substituted, and functionalized arenes as well as polycyclic aromatic hydrocarbons are selectively hydrogenated to obtain cyclohexane-based compounds under industrially viable and scalable conditions. The applicability of this hydrogenation methodology is presented for the storage of H2 in liquid organic hydrogen carriers.

Raney Ni-Al alloy-mediated reduction of alkylated phenols in water

Tan, Song-Liang,Liu, Guo-Bin,Gao, Xiang,Thiemann, Thies

experimental part, p. 5 - 7 (2009/09/06)

Raney Ni-Al alloy in a dilute aqueous alkaline solution has been shown to be a very powerful reducing agent in the hydrogenation of phenol and alkylated phenols to the corresponding cyclohexanol derivatives.

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