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84518-71-8

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84518-71-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 84518-71-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,5,1 and 8 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84518-71:
(7*8)+(6*4)+(5*5)+(4*1)+(3*8)+(2*7)+(1*1)=148
148 % 10 = 8
So 84518-71-8 is a valid CAS Registry Number.

84518-71-8SDS

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 bis-(4-methyl-cyclohexyl)-amine

1.2 Other means of identification

Product number -
Other names Bis-(4-methyl-cyclohexyl)-amin

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:84518-71-8 SDS

84518-71-8Downstream Products

84518-71-8Relevant articles and documents

Enhanced Selectivity in the Hydrogenation of Anilines to Cyclo-aliphatic Primary Amines over Lithium-Modified Ru/CNT Catalysts

Tomkins, Patrick,Müller, Thomas E.

, p. 1438 - 1445 (2018/03/30)

The hydrogenation of aromatic amines to the corresponding cycloaliphatic primary amines is an important industrial reaction. However, secondary amine formation and other side reactions are frequently observed, resulting in reduced selectivity. The side products are formed mostly on the support, yet support effects are little understood at present. This study describes the facile modification of Ru/CNT catalysts with LiOH, by this means significantly improving catalyst selectivity in toluidine hydrogenation without decreasing the activity of the catalysts. The effect is explained by LiOH diminishing acidic sites on the catalyst support and enhancing the adsorption of the aromatic ring on the metallic ruthenium nanoparticles. With the LiOH-modified Ru/CNT catalyst, other substrates, such as methylnitrobenzenes, are also converted efficiently. This study thus describes an improved catalyst for the preparation of cyclohexylamines and provides guidelines for future catalyst design.

Highly selective one-step hydrogenation of nitrobenzene to cyclohexylamine over the supported 10% Ni/carbon catalysts doped with 3‰ Rh

Lu, Xinhuan,Chen, Yang,Zhao, Zhenshuang,Deng, Hao,Zhou, Dan,Wei, Changcheng,Nie, Renfeng,Xia, Qinghua

, p. 15354 - 15361 (2016/02/26)

The carbon supported 10% Ni catalysts doped with 3‰ Rh have been prepared by an impregnation method. These catalysts have been used to catalyze the one-step hydrogenation of nitrobenzene to cyclohexylamine. The results show that the 3‰ Rh-10% Ni/CSC (biocarbon) catalyst exhibits an excellent performance to achieve 100 mol% conversion of nitrobenzene and 91.6% selectivity of cyclohexylamine under reaction conditions of 3.5 MPa and 140 °C. The recycling tests reveal recyclable stability of 3‰ Rh-10% Ni/CSC. This catalyst is active for the hydrogenation of a series of electron-deficient nitrobenzenes. Some factors such as the type of carriers, the content of Ni and Rh, the type of metals and additives play important roles in controlling the selective hydrogenation.

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