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6876-13-7

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6876-13-7 Usage

General Description

Cis-pinane is a bicyclic monoterpene commonly found in the essential oils of many plants, including various species of pine trees. It is a colorless liquid with a distinctly pine-like odor, and it is used in the fragrance industry as a scent additive in perfumes and household products. Cis-pinane is also utilized in the production of flavoring agents and as a precursor to other chemicals, such as camphor and synthetic carotenoids. Additionally, it has potential applications in the pharmaceutical and agrochemical industries due to its reported anti-inflammatory and insecticidal properties. Overall, cis-pinane is a versatile and commercially valuable compound with a range of practical uses.

Check Digit Verification of cas no

The CAS Registry Mumber 6876-13-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,8,7 and 6 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 6876-13:
(6*6)+(5*8)+(4*7)+(3*6)+(2*1)+(1*3)=127
127 % 10 = 7
So 6876-13-7 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/t7-,8-,9-/m0/s1

6876-13-7SDS

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 cis-Pinane

1.2 Other means of identification

Product number -
Other names (1S,2R,5S)-Pinane

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:6876-13-7 SDS

6876-13-7Relevant 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.]

Efficient and selective reduction of α-pinene to cis-pinane by NaBH4 using NiCl2?6H2O/PEG-800/ethanol as the catalytic system

Li, Kaoxue,Wang, Kang,Liu, Chuanchao,Yang, Xuhao,Chen, Xia,Ren, Yang,Cao, Shuhua,Liu, Meifang,Tai, Xishi,Li, Fahui

, p. 672 - 678 (2019/02/16)

The reduction of α-pinene by NaBH4 was achieved using NiCl2?6H2O in PEG-800/ethanol system under room temperature. Under the optimized conditions, the conversion of α-pinene and the selectivity of cis-pinane reached 97% and 98%, respectively. On the basis of TEM and a series of poisoning experiments, the nature of the active catalytic species for the reaction was discussed.

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.

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