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(4aS)-1,2,3,4,4aα,5,6,7,8,8aβ,9,9aβ,10,10aα-Tetradecahydroanthracene, also known as tetradecahydroanthracene, is a saturated hydrocarbon with the molecular formula C14H28. It is a cyclic compound with a 14-membered carbon ring, and its structure is similar to that of anthracene. This chemical is a colorless, flammable liquid with a faint odor. Tetradecahydroanthracene is primarily used as a starting material in the synthesis of other organic compounds, and it is also used as a solvent or a chemical intermediate in various industrial processes. Additionally, it is used in research and as a reference standard in analytical chemistry.

1755-19-7

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1755-19-7 Usage

Uses

Used in Chemical Synthesis:
Tetradecahydroanthracene is used as a starting material for the synthesis of other organic compounds. Its unique cyclic structure and saturated hydrocarbon nature make it a versatile building block for creating a wide range of chemical products.
Used in Industrial Processes:
As a solvent or chemical intermediate, tetradecahydroanthracene plays a crucial role in various industrial processes. Its ability to dissolve a variety of substances and act as a precursor for further chemical reactions contributes to its utility in this context.
Used in Research and Analytical Chemistry:
Tetradecahydroanthracene is also utilized in research settings and as a reference standard in analytical chemistry. Its distinct properties and structure make it an ideal candidate for studying chemical reactions and understanding the behavior of similar compounds.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, given its structural similarity to anthracene and its use in chemical synthesis, tetradecahydroanthracene could potentially be used in the development of pharmaceutical compounds, particularly those targeting specific biological pathways or receptors.
Used in Material Science:
Similarly, tetradecahydroanthracene's properties may also find applications in material science, where its unique structure could be leveraged to create novel materials with specific characteristics, such as improved stability or enhanced chemical reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 1755-19-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,7,5 and 5 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1755-19:
(6*1)+(5*7)+(4*5)+(3*5)+(2*1)+(1*9)=87
87 % 10 = 7
So 1755-19-7 is a valid CAS Registry Number.

1755-19-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (4aR,8aS,9aR,10aS)-PHA

1.2 Other means of identification

Product number -
Other names trans-syn-trans-Perhydroanthracen

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:1755-19-7 SDS

1755-19-7Relevant academic research and scientific papers

Hydrogenation of Anthracene and Dehydrogenation of Perhydroanthracene on Pt/C Catalysts

Kalenchuk,Koklin,Bogdan,Lunin

, p. 663 - 668 (2018/04/12)

The hydrogenation of anthracene on a heterogeneous catalyst containing 3 wt % Pt/C (Aldrich) at 215, 245, and 280°C and the pressures of 40 and 90 atm is studied. The hydrogenation of anthracene to a completely hydrogenated product is considered in detail

Deep hydrogenation of coal tar over a Ni/ZSM-5 catalyst

Qi, Shi-Chao,Zhang, Lu,Wei, Xian-Yong,Hayashi, Jun-Ichiro,Zong, Zhi-Min,Guo, Lu-Lu

, p. 17105 - 17109 (2014/05/06)

We have developed a Ni/ZSM-5 catalyst and utilised it to completely hydrogenate a series of condensed arenes, including naphthalene, anthracene and phenanthrene, under relatively mild conditions. The yields of decalin, perhydroanthracene and perhydrophenanthrene reached 100%, 98.8% and 25.8%, respectively. By analyzing the isomer distribution of the perhydroarenes, we proposed a mechanism of biatomic hydrogen transfer, which was further proven via the hydrogenation of 9,10-diphenylanthracene. Through hydrotreatment over the Ni/ZSM-5 catalyst, both high-temperature coal tar rich in condensed arenes and low-temperature coal tar mixing arenes with alkanes were greatly upgraded. The majority of arenes in the coal tars were deeply and even completely hydrogenated, which may open up a route for further processing and application of coal tar as clean fuels.

Stereoselective hydrogenation reactions in chloroaluminate(III) ionic liquids: A new method for the reduction of aromatic compounds

Adams, Christopher J.,Earle, Martyn J.,Seddon, Kenneth R.

, p. 1043 - 1044 (2007/10/03)

Stereoselective hydrogenation reactions in the ionic liquid system 1-ethyl-3-methylimidazolium chloride-AlCl3 can be performed with excellent yields and selectivities, using electropositive metals and a proton source.

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