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473-55-2

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473-55-2 Usage

Description

PINANE, also known as 1,2,3,4,4a,5,6,7-octahydropentalene, is a bicyclic monoterpene compound with a unique cage-like structure. It is a colorless liquid with a pungent odor and is insoluble in water but soluble in organic solvents. PINANE is synthesized through various chemical reactions and can be obtained from natural sources such as pine needles and other plant materials. Due to its unique chemical properties and structure, PINANE has found applications in various industries.

Uses

Used in Electronic Communication Industry:
PINANE is used as a component in the preparation method of heat-resistant connecting foam for electronic communication products. The heat-resistant connecting foam is essential for maintaining the integrity and performance of electronic components, especially in high-temperature environments. PINANE contributes to the foam's heat resistance, mechanical strength, and thermal stability, ensuring reliable connections and signal transmission in electronic communication devices.

Air & Water Reactions

Highly flammable. Insoluble in water.

Reactivity Profile

PINANE is incompatible with strong oxidizers.

Fire Hazard

PINANE is combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 473-55-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,7 and 3 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 473-55:
(5*4)+(4*7)+(3*3)+(2*5)+(1*5)=72
72 % 10 = 2
So 473-55-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H18/c1-7-4-5-8-6-9(7)10(8,2)3/h7-9H,4-6H2,1-3H3/t7u,8-,9-/m0/s1

473-55-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name pinane

1.2 Other means of identification

Product number -
Other names 2,6,6-trimethyl-bicyclo[3.1.1]heptan

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only. Intermediates,Odor agents
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:473-55-2 SDS

473-55-2Relevant articles and documents

The Exploration of Sensitive Factors for the Selective Hydrogenation of α-Pinene Over Recyclable Ni-B/KIT-6 Catalyst

Deng, Qiao,Hu, Tianding,Huang, Jinyan,Huang, Pengpeng,Jiang, Lihong,Shan, Shaoyun,Su, Hongying,Wang, Yaming,Yang, Wenjuan,Zheng, Yane,Zhi, Yunfei

, (2021/10/08)

The supported Ni-B/KIT-6 amorphous alloy catalyst was prepared by chemical reduction method for the hydrogenation reaction of α-pinene. The catalyst was characterized by XRD, BET, SEM–EDS, TEM, XPS, ICP and DLS, the influences of single factor of catalyst on its structure, morphology and performance were investigated and analyzed. It was found that the amount of Ni loading, preparation pH and B/Ni molar ratio had great effects on the reduction amount, dispersion and specific surface area of the catalyst, resulted in affecting the catalytic performance of the catalyst. The optimum synthesis conditions were at m(Ni2+)/m(KIT-6) = 1:3, pH 13 and n(B)/n(Ni) = 1.5, obtaining a 90.62% conversion of α-pinene and 97.67% selectivity of cis-pinane. In addition, the catalysts also exhibited better repeatability and stability. Graphic Abstract: [Figure not available: see fulltext.]

Colloid and Nanosized Catalysts in Organic Synthesis: XXII. Hydrogenation of Cycloolefins Catalyzed by Immobilized Transition Metals Nanoparticles in a Three-Phase System

Nebykov,Popov, Yu. V.,Mokhov,Latyshova,Shcherbakova,Nemtseva,Shishkin

, p. 1985 - 1989 (2019/11/29)

The processes of unsaturated cyclic hydrocarbons hydrogenation in a three-phase gas-liquid-solid catalyst system in the presence of nanostructured nickel, cobalt, or iron catalysts in a flow reactor at 130°C and atmospheric pressure have studied. RX3Extra activated carbon, γ-Al2O3, NaX zeolite, and Purolite CT-175 cation-exchange resin have been used as supports; NaBH4 and NH2NH2·H2O were used as reducing agents. The catalytic activity of supported nanoparticles and their selectivity with respect to the product of exhaustive hydrogenation have been investigated.

Highly selective and recyclable hydrogenation of α-pinene catalyzed by ruthenium nanoparticles loaded on amphiphilic core–shell magnetic nanomaterials

Wu, Fang-Zhu,Yu, Feng-Li,Yuan, Bing,Xie, Cong-Xia,Yu, Shi-Tao

, (2019/08/21)

A multifunctional nanomaterial (Fe3O4@SiO2@CX@NH2) comprising a magnetic core, a silicon protective interlayer, and an amphiphilic silica shell is successfully prepared. Ru nanoparticles catalyst loaded on Fe3O4@SiO2@CX@NH2 is used in hydrogenation of α-pinene for the first time. The novel nanomaterial with amphipathy can be used as a solid foaming agent to increase gas–liquid–solid three-phase contact and accelerate the reaction. Under the mild conditions (40?°C, 1?MPa H2, 3?h), 99.9% α-pinene conversion and 98.9% cis-pinane selectivity are obtained, which is by far the best results reported. Furthermore, the magnetic nanocomposite catalyst can be easily separated by an external magnet and reused nine times with high selectivity maintaining.

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